Care designed around your child’s digestive healt
Children’s digestive health is unique, so when your child experiences stomach issues, you need care you can trust. The pediatric gastroenterology team here at UTMB Health provides expert, compassionate support for a range of conditions, including common feeding and growth issues, upper GI disorders, and motility disorders. We focus on making kids comfortable and helping them feel their best so they can grow and thrive.
Conditions We Treat
Feeding & Growth Issues
Celiac Disease
Overview:
Celiac disease is an autoimmune disorder where the body reacts to gluten (a protein in wheat, rye, and barley). This reaction damages the small intestine lining and prevents nutrient absorption. It can appear at any age and tends to run in families. Long-term, untreated celiac disease can lead to malnutrition and other health problems.
Common Symptoms:
- Diarrhea or constipation
- Abdominal pain or bloating
- Unexplained weight loss
- Fatigue
- Skin rash
Treatments & Procedures:
- Lifelong gluten-free diet
- Nutritional counseling
- Supplements for vitamin and mineral deficiencies
- Regular monitoring with blood tests
- Supportive care for associated conditions
Cow’s Milk Protein Intolerance
Overview:
Cow's Milk Protein Intolerance is a condition in which the immune system reacts to proteins found in cow’s milk, typically through a delayed, non-IgE–mediated response. It most commonly affects infants and young children and involves difficulty processing milk proteins. The condition is often temporary and may resolve as the digestive and immune systems mature.
Common Symptoms:
- Vomiting
- Diarrhea or loose stools
- Blood or mucus in stool
- Abdominal discomfort
- Colic-like irritability
- Poor feeding
Treatments & Procedures:
- Elimination of cow’s milk protein from diet
- Use of extensively hydrolyzed or amino acid-based formulas
- Maternal dietary modification (if breastfeeding)
- Gradual reintroduction under medical guidance
- Nutritional monitoring
Eosinophilic Esophagitis (EoE)
Overview:
Eosinophilic esophagitis (EoE) is a chronic immune-mediated disorder affecting the esophagus, often triggered by certain foods or environmental allergens. It involves an elevated number of eosinophils, a type of white blood cell, in the esophageal lining. Over time, this inflammation can lead to structural changes that affect how the esophagus functions and responds to swallowed food.
Common Symptoms:
- Difficulty swallowing (dysphagia)
- Food getting stuck in the esophagus (food impaction)
- Chest discomfort or pain
- Persistent heartburn or reflux symptoms
- Feeding difficulties in children
- Poor growth in pediatric cases
Treatments & Procedures:
- Dietary elimination (removal of trigger foods)
- Proton pump inhibitor (PPI) therapy
- Topical corticosteroids (swallowed medications)
- Esophageal dilation (for narrowing/strictures)
- Ongoing monitoring with endoscopy and biopsy
Failure to Thrive/Poor Weight Gain
Overview:
Failure to thrive describes when a child is not gaining weight or growing as expected. This can result from medical conditions, nutritional issues, or feeding challenges. Pediatric gastroenterologists assess feeding patterns, absorption, and overall health to identify causes and create individualized plans that promote healthy growth and development. Early intervention helps children reach their full potential.
Common Symptoms
- Slow or stagnant weight gain
- Growth below expected curve
- Frequent feeding difficulties
Treatments & Procedures:
- Nutritional assessment and counseling
- High-calorie or special diets
- Feeding therapy support
- Evaluation for underlying GI or metabolic conditions
Feeding & Swallowing Difficulties
Overview:
Feeding and swallowing difficulties may arise from developmental, structural, or neurological conditions. These challenges can affect nutrition, growth, and a child’s relationship with food. Pediatric gastroenterologists work with feeding specialists, speech-language pathologists, and dietitians to identify causes and create care plans that make eating safer and more enjoyable for children.
Common Symptoms:
- Choking or gagging with food
- Refusal to eat certain textures
- Prolonged feeding times
- Poor growth or weight gain
Treatments & Procedures:
- Upper endoscopy with biopsies
- Swallow studies and imaging
- Feeding therapy with specialists
- Modified diets or thickened liquids
- Feeding tubes if needed
Upper GI Disorders
Congenital Anomalies of the GI Tract
Overview:
Congenital anomalies of the gastrointestinal tract are structural or functional abnormalities present at birth that affect how the digestive system develops and works. These may involve the esophagus, stomach, intestines, liver, or bile ducts. Some are detected soon after birth, while others appear later in childhood. Early diagnosis and specialized surgical or medical care can help children lead healthy, active lives.
Common Symptoms:
- Feeding difficulties or vomiting
- Abdominal distension or pain
- Poor weight gain or growth delays
- Jaundice (yellowing of the skin or eyes)
- Chronic constipation or diarrhea
- Difficulty swallowing
- Signs of intestinal blockage (no stool, swollen abdomen, irritability)
Treatments & Procedures:
- Diagnostic imaging (ultrasound, X-ray, or MRI)
- Endoscopic evaluation to assess or treat structural issues
- Surgical repair of defects such as atresia, malrotation, or fistula
- Nutritional support and feeding therapy
- Ongoing monitoring by pediatric gastroenterologists and surgeons
- Coordinated multidisciplinary care to support growth and development
Eosinophilic Esophagitis (EoE)
Overview:
Eosinophilic esophagitis (EoE) is a chronic immune-mediated disorder affecting the esophagus, often triggered by certain foods or environmental allergens. It involves an elevated number of eosinophils, a type of white blood cell, in the esophageal lining. Over time, this inflammation can lead to structural changes that affect how the esophagus functions and responds to swallowed food.
Common Symptoms:
- Difficulty swallowing (dysphagia)
- Food getting stuck in the esophagus (food impaction)
- Chest discomfort or pain
- Persistent heartburn or reflux symptoms
- Feeding difficulties in children
- Poor growth in pediatric cases
Treatments & Procedures:
- Dietary elimination (removal of trigger foods)
- Proton pump inhibitor (PPI) therapy
- Topical corticosteroids (swallowed medications)
- Esophageal dilation (for narrowing/strictures)
- Ongoing monitoring with endoscopy and biopsy
Esophageal Strictures & Motility Disorders
Overview:
Esophageal strictures and motility disorders affect how food moves from the mouth to the stomach. Strictures occur when the esophagus narrows, often from inflammation, acid reflux, or scarring. Motility disorders, such as achalasia or esophageal spasm, involve abnormal muscle movement. These conditions can cause swallowing difficulties and discomfort but are treatable with specialized evaluation and minimally invasive therapies.
Common Symptoms:
- Difficulty swallowing (dysphagia)
- Chest pain or pressure after eating
- Regurgitation of food or liquids
- Heartburn or acid reflux
- Unintentional weight loss
- Coughing or choking while eating
- Sensation of food “sticking” in the throat or chest
Treatments & Procedures:
- Upper endoscopy for diagnosis and treatment
- Esophageal dilation to widen strictures
- Medications to reduce acid reflux or inflammation
- Esophageal manometry (for achalasia)
- Dietary modifications and swallowing therapy
- Ongoing monitoring by a gastroenterologist or motility specialist
Gastroesophageal Reflux Disease (GERD) - Pediatric
Overview:
GERD occurs when stomach contents flow back into the esophagus often enough to cause irritation or complications. While reflux is common in infants, persistent GERD can affect growth, feeding, and comfort. Pediatric gastroenterologists use a combination of evaluation, lifestyle guidance, and medication to control acid exposure and protect long-term digestive health.
Common Symptoms:
- Frequent vomiting or spit-up
- Irritability with feeding
- Poor weight gain
- Cough or throat discomfort
Treatments & Procedures:
- Feeding and lifestyle changes
- Acid-reducing medications
- Endoscopy in certain cases
- Surgery for severe or resistant cases
Inflammatory & Functional Bowel Diseases
Constipation & Fecal Incontinence
Overview:
Constipation and fecal incontinence are closely linked conditions, most common in children but also seen in adults. Chronic constipation can cause stool buildup in the colon, stretching the bowel and leading to leakage of softer stool around the blockage, known as encopresis or fecal incontinence. Early diagnosis, consistent management, and supportive care help restore normal bowel habits and prevent long-term complications.
Common Symptoms:
- Infrequent or difficult bowel movements
- Hard, dry, or painful stools
- Abdominal pain or bloating
- Stool leakage or soiling (especially in children)
- Loss of appetite or nausea
- Withholding behavior or fear of using the toilet
- Feeling of incomplete bowel emptying
Treatments & Procedures:
- Dietary changes to increase fiber and hydration
- Stool softeners or mild laxatives under medical guidance
- Scheduled toileting routines and positive reinforcement
- Education for families on healthy bowel habits
- Pelvic floor or biofeedback therapy (for older children or adults)
- Behavioral counseling when withholding or anxiety is involved
- Ongoing follow-up with a gastroenterologist for chronic cases
Inflammatory Bowel Disease (IBD)
Overview:
Inflammatory bowel disease (IBD) is a chronic condition that causes inflammation in the digestive tract, primarily including Crohn’s disease and ulcerative colitis. These disorders can lead to ongoing abdominal pain, diarrhea, and fatigue. While IBD has no known cure, advanced medical and surgical treatments help manage inflammation, reduce flare-ups, and improve long-term quality of life for both adults and children.
Common Symptoms:
- Abdominal pain and cramping
- Chronic diarrhea (sometimes with blood or mucus)
- Urgent or frequent bowel movements
- Fatigue and low energy
- Unintended weight loss
- Fever during flare-ups
- Reduced appetite
- In severe cases, anemia or joint pain
Treatments & Procedures:
- Medications for inflammation and flare management
- Infusion therapy: biologics, such as infliximab or vedolizumab, to target immune response
- Corticosteroids for short-term flare control
- Nutritional therapy and dietary support
- Endoscopic evaluation and monitoring
- Surgery for complications such as strictures or fistulas
Unexplained Abdominal Pain or Bloating
Overview:
Ongoing abdominal pain or bloating without a clear cause may be linked to digestive conditions such as irritable bowel syndrome (IBS), food intolerances, or more serious gastrointestinal (GI) disorders. Careful evaluation helps rule out underlying causes and provides relief strategies.
Common Symptoms:
- Abdominal discomfort or cramping
- Fullness or swelling
- Gas
- Changes in bowel habits
- Pain that comes and goes
Treatments & Procedures:
- Dietary changes (low FODMAP, avoid triggers)
- Medications for IBS or digestive issues
- Stress management techniques
- Probiotics
- Diagnostic testing to identify causes
Liver, Pancreas, & Biliary Disorders
Cirrhosis & Metabolic Liver Diseases
Overview:
Cirrhosis and metabolic liver diseases involve chronic liver damage that leads to scarring, impaired function, and potential complications. Causes may include chronic hepatitis, genetic enzyme disorders, or bile flow obstruction. These conditions can affect both children and adults. Early diagnosis, nutritional support, and targeted treatments can help slow disease progression and maintain liver health.
Common Symptoms:
- Fatigue and weakness
- Jaundice and dark urine
- Abdominal swelling (ascites)
- Easy bruising or bleeding
- Poor appetite or weight loss
- Confusion or irritability (from toxin buildup)
Treatments & Procedures:
- Laboratory tests and imaging to monitor liver function
- Medications to manage underlying metabolic or inflammatory causes
- Nutritional and vitamin supplementation
- Endoscopic or surgical treatment for complications (varices, ascites)
- Liver transplant evaluation for advanced disease
- Ongoing care by hepatology and metabolic specialists
Congenital Biliary Diseases
Overview:
Congenital biliary diseases, such as biliary atresia, affect the bile ducts, preventing normal bile flow from the liver to the intestine. This leads to liver damage and jaundice in infants. Biliary atresia is a serious condition requiring early diagnosis and surgical treatment to preserve liver function. Ongoing medical care supports digestion, growth, and long-term liver health.
Common Symptoms:
- Persistent jaundice beyond two weeks of age
- Pale or clay-colored stools
- Dark urine
- Enlarged liver or spleen
- Poor weight gain or feeding issues
- Irritability or fatigue
Treatments & Procedures:
- Blood tests and imaging to assess bile ducts
- Kasai portoenterostomy surgery to restore bile flow
- Nutritional support and fat-soluble vitamin supplementation
- Medications to improve bile drainage and reduce itching
Hepatitis - Pediatric
Overview:
Hepatitis refers to inflammation of the liver caused by viral infections, autoimmune reactions, medications, or toxins. In children, viral hepatitis (A, B, C, D, or E) is most common and can affect liver function and overall health. Early detection, vaccination, and appropriate treatment help prevent complications such as chronic liver disease and ensure healthy growth and recovery.
Common Symptoms:
- Fatigue or weakness
- Jaundice (yellowing of the skin or eyes)
- Abdominal pain or swelling
- Dark urine and pale stools
- Nausea, vomiting, or loss of appetite
- Fever or flu-like symptoms
Treatments & Procedures:
- Blood tests to determine hepatitis type and liver function
- Antiviral or immune-modulating medications (for chronic hepatitis)
- Supportive care for acute viral hepatitis
- Vaccination for prevention (Hepatitis A and B)
- Regular monitoring for liver inflammation or fibrosis
- Nutritional support and lifestyle guidance
Neonatal Jaundice & Cholestasis
Overview:
Neonatal jaundice and cholestasis both involve elevated bilirubin levels that cause yellowing of a newborn’s skin and eyes. While jaundice is common and often harmless, cholestasis indicates reduced or blocked bile flow from the liver and may signal a more serious condition. Early evaluation helps distinguish between the two, ensuring timely treatment to prevent liver damage and promote healthy development.
Common Symptoms:
- Yellowing of the skin and eyes (jaundice)
- Dark urine and pale or clay-colored stools
- Poor feeding or irritability
- Fatigue or sluggishness
- Abdominal swelling or tenderness
- Slow weight gain or growth problems
- Persistent jaundice lasting beyond two weeks of life
Treatments & Procedures:
- Blood tests to measure bilirubin and liver function
- Phototherapy for physiologic jaundice
- Ultrasound or imaging to assess liver and bile ducts
- Nutritional and vitamin support (especially fat-soluble vitamins)
- Medications to improve bile flow or reduce itching
- Surgery for underlying causes such as biliary atresia
- Ongoing care by pediatric gastroenterologists
Pancreatitis - Pediatric
Overview:
Pancreatitis in children is the inflammation of the pancreas, a gland that helps with digestion and blood sugar control. It can be acute, developing suddenly, or chronic, occurring over time with repeated inflammation. Causes in children often include infections, certain medications, abdominal injury, or genetic conditions. Early diagnosis and management are important to prevent complications and long-term pancreatic damage.
Common Symptoms:
- Abdominal pain (often in upper or middle abdomen)
- Nausea or vomiting
- Fever
- Abdominal tenderness or swelling
- Poor appetite or irritability (especially in younger children)
Treatments & Procedures:
Treatment focuses on supportive care, including IV fluids, pain control, and bowel rest until symptoms improve. The underlying cause, such as infection, medication, or anatomical abnormality, is addressed directly. Nutritional support may include gradual reintroduction of food or tube feeding if needed. In complex cases, procedures like MRI or surgery may be used for diagnosis or to correct structural issues.
Malabsorption & Nutritional Disorders
Celiac Disease
Overview:
Celiac disease is an autoimmune disorder where the body reacts to gluten (a protein in wheat, rye, and barley). This reaction damages the small intestine lining and prevents nutrient absorption. It can appear at any age and tends to run in families. Long-term, untreated celiac disease can lead to malnutrition and other health problems.
Common Symptoms:
- Diarrhea or constipation
- Abdominal pain or bloating
- Unexplained weight loss
- Fatigue
- Skin rash
Treatments & Procedures:
- Lifelong gluten-free diet
- Nutritional counseling
- Supplements for vitamin and mineral deficiencies
- Regular monitoring with blood tests
- Supportive care for associated conditions
Congenital Anomalies of the GI Tract
Overview:
Congenital anomalies of the gastrointestinal tract are structural or functional abnormalities present at birth that affect how the digestive system develops and works. These may involve the esophagus, stomach, intestines, liver, or bile ducts. Some are detected soon after birth, while others appear later in childhood. Early diagnosis and specialized surgical or medical care can help children lead healthy, active lives.
Common Symptoms:
- Feeding difficulties or vomiting
- Abdominal distension or pain
- Poor weight gain or growth delays
- Jaundice (yellowing of the skin or eyes)
- Chronic constipation or diarrhea
- Difficulty swallowing
- Signs of intestinal blockage (no stool, swollen abdomen, irritability)
Treatments & Procedures:
- Diagnostic imaging (ultrasound, X-ray, or MRI)
- Endoscopic evaluation to assess or treat structural issues
- Surgical repair of defects such as atresia, malrotation, or fistula
- Nutritional support and feeding therapy
- Ongoing monitoring by pediatric gastroenterologists and surgeons
- Coordinated multidisciplinary care to support growth and development
Genetic Metabolic Conditions
Overview:
Genetic metabolic conditions are inherited disorders that affect how the body processes nutrients and produces energy. These conditions can interfere with the breakdown of proteins, fats, or carbohydrates, leading to imbalances that impact growth, development, and organ function. Early detection, dietary management, and specialized medical care help prevent serious complications and support long-term health in infants, children, and adults.
Common Symptoms:
- Poor feeding or vomiting
- Slow growth or weight gain
- Low blood sugar (hypoglycemia)
- Fatigue or weakness
- Developmental delays
- Muscle stiffness or low tone
- Digestive problems such as diarrhea or bloating
- Periods of illness-related metabolic “crisis”
Treatments & Procedures:
- Newborn screening and genetic testing for early diagnosis
- Personalized nutrition plans or restricted diets
- Vitamin, mineral, or amino acid supplementation
- Medications to correct or support metabolic function
- Regular blood and organ function monitoring
- Emergency protocols during illness or stress
- Ongoing multidisciplinary care with metabolic, nutrition, and gastroenterology specialists
Lactose Intolerance
Overview:
Lactose intolerance occurs when the body has difficulty digesting lactose, the natural sugar in milk and dairy products. While not dangerous, it can cause discomfort and limit food choices. Pediatric gastroenterologists help confirm the diagnosis and guide families on how to manage symptoms while still ensuring children receive enough calcium and nutrients for healthy growth.
Common Symptoms
- Bloating or gas after dairy
- Diarrhea
- Abdominal cramps
- Nausea
Treatments & Procedures:
- Lactose-free diet or dairy alternatives
- Lactase enzyme supplements
- Nutrition counseling for calcium and vitamin D
- Breath testing for diagnosis
Short Bowel Syndrome - Pediatric
Overview:
Short bowel syndrome occurs when a significant portion of the small intestine is missing or not working properly, often after surgery for congenital or acquired conditions. This leads to difficulty absorbing nutrients and fluids. Pediatric gastroenterologists provide specialized care, often involving advanced nutrition support, to help children grow and thrive while managing this complex condition.
Common Symptoms
- Poor nutrient absorption
- Chronic diarrhea
- Dehydration risk
- Growth delays
Treatments & Procedures:
- Intravenous or tube feeding (parenteral/enteral nutrition)
- Specialized diets
- Medications to slow bowel movement or improve absorption
Motility Disorders
Chronic Intestinal Pseudo-Obstruction (CIPO)
Overview:
Chronic intestinal pseudo-obstruction (CIPO) is a rare disorder where the intestines act as though they are blocked, but no physical obstruction is present. Instead, nerve or muscle dysfunction prevents normal motility. It may be congenital or develop later in life due to systemic disease or injury. CIPO can be severe and require long-term care.
Common Symptoms
- Abdominal pain and bloating
- Nausea and vomiting
- Severe constipation or diarrhea
- Malnutrition and weight loss
- Symptoms mimicking bowel obstruction
Treatments & Procedures:
- Nutritional support, including IV nutrition in severe cases
- Medications to stimulate motility or relieve symptoms
- Decompression with tubes to relieve pressure
- Surgery for complications, though often limited benefit
Gastroparesis
Overview:
Gastroparesis is delayed stomach emptying due to weakened stomach muscles or nerve damage, often linked to diabetes, surgery, or certain medications. Food remains in the stomach longer than normal, leading to nausea, bloating, and nutritional issues. It can be chronic and requires careful management.
Common Symptoms:
- Early fullness after small meals
- Nausea and vomiting
- Abdominal bloating or pain
- Weight loss and poor appetite
- Fluctuating blood sugars in people with diabetes
Treatments & Procedures:
- Dietary changes (small, frequent meals; low-fat, low-fiber foods)
- Medications that improve stomach motility (prokinetics)
- Anti-nausea medications
- Feeding tubes or gastric electrical stimulation for severe cases
Hirschsprung's Disease
Overview:
Hirschsprung's disease, also known as congenital aganglionic megacolon, happens when certain nerve cells (ganglion cells) in an infant's intestines do not form correctly, leading to a slowdown in the movement of stool through the intestines. Timely diagnosis and treatment are vital for addressing Hirschsprung's disease, which may manifest in newborns with symptoms like intestinal blockage or an infection called enterocolitis.
Symptoms may include:
- Newborns:
- not having a bowel movement within the first 48 hours of life
- swelling of the belly
- vomiting
- constipation or gas, which can make them very fussy
- Older children:
- ongoing constipation
- a swollen belly
- lack of appetite
- poor growth
Treatment/procedure options:
The main treatment for Hirschsprung's disease is surgical removal of the part of the colon that lacks nerve cells. After removing the affected section, the surgeon attaches the healthy part of the colon to the anus, allowing normal bowel movements. This surgery can sometimes be done in one step, but some children may need a temporary ostomy. An ostomy is a surgery that creates an opening in the abdomen for stool to exit into a special bag; it may be necessary if the colon needs time to heal or if the surgery is done in two steps.
Other Conditions
Gastrointestinal Bleeding (GI Bleeds)
Overview:
Gastrointestinal (GI) bleeding occurs when bleeding happens anywhere along the digestive tract, from the mouth to the rectum. It can range from mild to life-threatening and may appear as visible blood in vomit or stool, or be hidden and detected through tests. Causes vary by age but may include ulcers, tears, inflammation, or vascular abnormalities. Prompt diagnosis and treatment are essential to prevent serious complications.
Common Symptoms:
- Vomiting blood (bright red or resembling coffee grounds)
- Black, tarry stools or bright red blood in stool
- Abdominal pain or cramping
- Fatigue, dizziness, or fainting
- Pale skin or signs of anemia
Treatments & Procedures:
Treatment depends on the source and severity of the bleeding. Initial care focuses on stabilizing the patient with IV fluids, blood transfusions if necessary, and monitoring vital signs.
- Endoscopy is the main diagnostic and treatment procedure, allowing doctors to locate and control bleeding with clips, cautery, or injections.
- Colonoscopy is used for lower GI bleeding.
- Medications may include proton pump inhibitors (for ulcers) or antibiotics (for infections).
- In severe or persistent cases, angiography or surgery may be required to repair damaged blood vessels or remove affected tissue.
Genetic & Rare GI Diseases in Children
Overview:
Genetic and rare gastrointestinal (GI) diseases in children are uncommon disorders caused by inherited or spontaneous genetic changes that affect how the digestive system functions. These conditions can involve the stomach, intestines, liver, or pancreas and often lead to problems with digestion, absorption, or motility. Early diagnosis through genetic testing and specialized evaluation is important to manage symptoms, support growth, and prevent complications.
Common Symptoms:
- Poor growth or failure to thrive
- Chronic diarrhea or constipation
- Abdominal pain or bloating
- Vomiting or feeding difficulties
- Nutrient deficiencies or weight loss
- Unusual stool color, texture, or frequency
Treatments & Procedures:
Treatment focuses on managing symptoms, improving nutrition, and addressing the underlying genetic cause when possible.
- Nutritional therapy: special diets, enzyme replacement, or supplemental feeding to ensure proper growth.
- Medications: to control inflammation, improve motility, or support digestion.
- Genetic counseling: helps families understand inheritance patterns and future risks.
- Diagnostic procedures: may include endoscopy, colonoscopy, or imaging studies to evaluate intestinal function and structure.
- In severe or progressive cases, surgery or organ transplantation (such as liver or intestine) may be considered.
Your Care Team
Each provider may treat different conditions. Click on a profile to see their areas of specialty.
Frequently Asked Questions.
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When should I take my child to a pediatric gastroenterologist?
If your child has ongoing digestive problems such as frequent abdominal pain, constipation, diarrhea, poor weight gain, trouble swallowing, or unexplained vomiting, a referral to a pediatric gastroenterologist may be helpful.
-
How are pediatric digestive conditions diagnosed?
Doctors use a combination of medical history, physical exams, blood or stool tests, imaging studies, and sometimes procedures like endoscopy or colonoscopy to get a clear understanding of your child’s digestive health.
-
What treatments are available for children’s digestive problems?
Treatment depends on the condition but may include nutrition and diet plans, medications, behavioral strategies, or in some cases, procedures or surgery. Our team provides a personalized care plan for each child.
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Will my child need special diets if they have a GI condition?
Some conditions, such as celiac disease, food allergies, or lactose intolerance, require dietary adjustments. Our team includes nutrition experts who work with families to create safe, balanced meal plans that support growth.
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Are digestive issues common in children?
Yes. Digestive issues such as constipation, reflux, abdominal pain, and food sensitivities are very common in kids. Most are manageable with the right care, and many improve with time and support.
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Can digestive problems affect my child’s growth?
Yes, conditions that interfere with nutrition or absorption can impact growth. Early evaluation and treatment help children catch up and stay on a healthy growth track.
All Gastroenterology Specialties
Our Locations
- 400 Harborside Drive
Suite 103 - M–F: 7:30 a.m.–5:30 p.m.
- (409) 772-3695
- (409) 772-3680
- Website
- 250 Blossom Street
4th Floor - M–F: 8 a.m.–5 p.m.
- (409) 772-3695 or (888) 886-2543
- (409) 772-3680
- Website