Mucopolysaccharidosis 2
Skeletal irregularities, vision problems, heart problems, diarrhea, joint stiffness, stunted growth and delayed development may be present.[symptoma.com]
[…] resulting in large rounded cheeks and thick lips – generally manifests between ages 18 months and four years in the early progressive form and about two years later for those[ncbi.nlm.nih.gov]
Initial manifestations include: frequent respiratory tract infections (in particular otitis media); umbilical and inguinal hernia; intractable diarrhea; hepatosplenomegaly[orpha.net]
Mucopolysaccharidosis
Cardiac involvement is common in MPS patients and usually consists of progressive valvular thickening with incompetence and cardiomyopathy.[ncbi.nlm.nih.gov]
The most frequently reported adverse reactions included: chills, vomiting, nausea, arthralgia, diarrhea, tachycardia, abdominal pain, blood pressure increased, and oxygen[biomarin.com]
[…] mucopolysaccharidosis type VI) is a rare lysosomal storage disorder in which the pathologic storage of glycosaminoglycans in various tissues can lead to severe symptoms, including cardiomyopathy[ncbi.nlm.nih.gov]
Mucopolysaccharidosis 1
Diet A dietician can help you create a nutrition plan to help your baby control diarrhea and constipation, which may occur in those with severe MPS I.[babysfirsttest.org]
Cardiomyopathy and coronary heart disease. Hepatosplenomegaly.[patient.info]
The most frequently reported adverse reactions included: chills, vomiting, nausea, arthralgia, diarrhea, tachycardia, abdominal pain, blood pressure increased, and oxygen[biomarin.com]
Barth Syndrome
Diarrhea and/or constipation. Weak muscle tone may lead to fatigue and difficulty exercising.[news-medical.net]
Barth Syndrome - X-linked Cardiomyopathy and Neutropenia Richard I.[web.archive.org]
face with full cheeks, broad forehead, prominent chin, large ears and deep-set eyes What are the causes of Barth syndrome?[childrenshospital.org]
Fabry Disease
Gastrointestinal signs and symptoms-abdominal pain, nausea, diarrhea and diverticular disease--are some of the most frequently reported complaints in patients with Fabry disease[ncbi.nlm.nih.gov]
KEYWORDS: Fabry disease; cardiomyopathy, hypertrophic; gadolinium; magnetic resonance; mutation; phenotype; stroke[ncbi.nlm.nih.gov]
Round-robin slide reviews and two face-to-face scoring sessions with a modified Delphi technique [ 23 ] were used to refine the scoring system.[ncbi.nlm.nih.gov]
Amyloidosis
Pedigree of Family with a PRNP Y163X Mutation Associated with Chronic Diarrhea and Autonomic Failure.[doi.org]
Echocardiogram and cardiac MRI scan showed restrictive cardiomyopathy. Congo red staining of gastric biopsies showed amyloid deposition.[ncbi.nlm.nih.gov]
Weight gain and rounded face. Muscle weakness (uncommon when used intermittently as for treating amyloidosis). Vaginal yeast infection.[ahajournals.org]
Mushroom Poisoning
The typical symptoms of nausea, vomiting, abdominal pain, and diarrhea are nonspecific and can be mistaken for gastroenteritis.[ncbi.nlm.nih.gov]
Possible sequelae include cardiomyopathy, coagulopathy, and seizures (1,2,5).[cdc.gov]
A polygonal spore with more than six faces (a cube has 6 faces) is called "prismatic" (Fig. 32). A nearly cubic spore is called "rhomboid."[web.archive.org]
Malnutrition
The double insult of IBD and GBP resulted in severe malnutrition, with a serum albumin concentration of 0.9 g/dL (reference range, 3.5 to 5.0), weight loss, and watery diarrhea[ncbi.nlm.nih.gov]
Carnitine nutritional deficiency Decreased nutritional requirement Deficiency of macronutrients Deficiency of micronutrients Dietary potassium - low Dietary sodium - low Dilated cardiomyopathy[icd9data.com]
Face appears round with swollen abdomen and legs. Skin is dry and dark with splits or stretch marks like streaks where stretched.[news-medical.net]
Duodenal Carcinoid Syndrome
Diarrhea, Chronic is a topic covered in the 5-Minute Clinical Consult.[unboundmedicine.com]
Takotsubo cardiomyopathy: A unique cardiomyopathy with variable ventricular morphology. JACC Cardiovasc Imaging. 2010; 3 :641–649. [ PubMed ] [ Google Scholar ] 17.[ncbi.nlm.nih.gov]
An initial draft document was produced and subsequently reviewed and modified in accordance with the AGREE tool. 1 Two face-to-face meetings as well as a further two telephone[gut.bmj.com]
Congenital Muscular Dystrophy
During the infancy, the child suffered from unexplained diarrhea and failure to thrive.[doi.org]
cardiomyopathy died at the ages of 2 years 1 month, and 7 years 4 months respectively.[ncbi.nlm.nih.gov]
, Congenital cataract and cardiomyopathy, Dilated cardiomyopathy (DCM), Myopathy, myofibrillar, Cataract 16, multiple types, Myopathy, myofibrillar, fatal infantile hypertonic[blueprintgenetics.com]