About Congenital Tufting Enteropathy

Diarrhea 5, with Tufting Enteropathy, Congenital, also known as congenital diarrhea 5 with tufting enteropathy, is related to diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies and intestinal atresia, and has symptoms including infantile diarrhea An important gene associated with Diarrhea 5, with Tufting Enteropathy, Congenital is EPCAM (Epithelial Cell Adhesion Molecule), and among its related pathways/superpathways is CFTR-dependent regulation of ion channels in Airway Epithelium (norm and CF). The drugs Fluorouracil and Levoleucovorin have been mentioned in the context of this disorder. Affiliated tissues include small intestine, brain and liver, and related phenotypes are failure to thrive and chronic diarrhea

Major Symptoms of Congenital Tufting Enteropathy

Congenital tufting enteropathy (CTE) is a rare genetic disorder that affects the development and function of the small intestine. The major symptoms of CTE include constipation, vomiting, abdominal pain and discomfort, and a decreased appetite.

Suitable Lifestyle for People with Congenital Tufting Enteropathy

Congenital tufting enteropathy (CTE) is a rare genetic disorder that affects the development and function of the cilium, a thin layer of muscle tissue in the interstitial space. This condition can cause a range of symptoms, including gastrointestinal problems, such as constipation, vomiting, and diarrhea. In terms of lifestyle, it is important for patients with CTE to follow a specific diet that is high in fiber and low in fat and added sugars. This diet can help manage the symptoms of CTE and improve overall health. Patients with CTE should also avoid activities that can put stress on the gastrointestinal tract, such as heavy physical exercise or prolonged sitting. It is recommended that patients with CTE seek medical advice and work closely with a healthcare professional to develop a personalized treatment plan that addresses their specific needs and manages their symptoms.

Other Diseases

Chronic Enteropathy Associated with SLCO2A1 GeneCongenital DysfibrinogenemiaCongenital MyopathyCongenital TorticollisCongenital AfibrinogenemiaCongenital AniridiaCongenital PoikilodermaCongenital NystagmusCongenital GlaucomaCongenital AnosmiaCongenital ChylothoraxCongenital HypofibrinogenemiaCongenital ChloridorrheaCongenital Sodium DiarrheaCongenital Ichthyosiform ErythrodermaCongenital Adrenal Hyperplasia 1Congenital Disorders of GlycosylationCongenital Dyserythropoietic AnemiaCongenital Diaphragmatic HerniaCongenital Muscular Dystrophy