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98 Possible Causes for Congenital Alopecia, Short Bowel Syndrome, Zinc Deficiency

  • Brandt Syndrome

    Rupture of blisters expose the purulent eroded skin lesions. [1,2,4] Alopecia Diffuse hair loss in scalp, eye lashes and eye brows can be seen.[] bowel syndrome due to multiple small bowel obstructions with subsequent bowel resections who was on chronic total parenteral nutrition (TPN) presented with bullae on the[] Discovering genetic causes of zinc deficiency has been a remarkable scientific journey.[]

  • Zinc Deficiency

    Malnutrition, prematurity, total parenteral nutrition dependence, and burns increase the demand for zinc, whereas congenital malabsorption syndromes represent clinical situations[] […] diseases such as ulcerative colitis and Crohn’s disease, and nutrient absorption syndromes such as short bowel syndrome and celiac disease.[] Diagnosis: Measuring the plasma zinc levels helps in diagnosis of zinc deficiency.[]

  • Celiac Disease

    syndrome Peripheral neuropathy Recurrent migraine Selective immunoglobulin A deficiency Short stature (in children) Sjögren's syndrome Turner's syndrome Type 1 diabetes mellitus[] Work-up revealed iron deficiency anemia, zinc deficiency and an abnormal celiac panel.[] Congenital heart defects Primary biliary cirrhosis IgA deficiency Isolated hypertransaminasemia Recurrent aphthous stomatitis Myasthenia gravis Recurrent pericarditis Psoriasis[]

  • Hypothyroidism

    […] of the puppy coat, hyperpigmentation of the skin, and bilaterally symmetric alopecia of the trunk.[] Short bowel syndrome (SBS) is the leading cause of intestinal failure in children, a condition of absence of sufficient bowel to meet the nutritional and metabolic needs of[] While zinc deficiency is very uncommon in the developed world, it’s still recommended to eat a variety of zinc-rich foods ( 8 ).[]

  • Erythroderma Desquamativum

    Setleis Syndrome Severe Combined Immunodeficiency Sheehan syndrome Short Bowel Syndrome Short Chain Acyl CoA Dehydrogenase Deficiency (SCAD) SHORT Syndrome Shwachman Syndrome[] […] enzyme that may serve as surrogate diagnostic marker of zinc deficiency.[] Alopecia and Nail Dystrophy *601863 Regulatory Factor 5; RFX5 *602450 Severe Combined Immunodeficiency, Athabascan Type; SCIDA *602667 Nijmegen Breakage Syndrome Gene; NBS1[]

  • Oculo-Osteo-Cutaneous Syndrome

    3.5ORPHA Number Disease or group of diseasesEstimated prevalence (/100,000)792 X-linked retinoschisis 3.52103 Guillain-Barr syndrome 3.45117 Behcet disease 3.4104008 Short[] Alopecia 2 Palmoplantar Keratoderma and Congenital Alopecia, Autosomal Dominant Papillon-Lefevre Syndrome Pili Torti and Developmental Delay Pilodental Dysplasia with Refractive[] 3.45 116 Beckwith-Wiedemann syndrome 2.3**104008 Short bowel syndrome 3.4 6 Isolated 3-methylcrotonyl-CoA carboxylase deficiency 2.3**75377 Central areolar choroidal dystrophy[]

  • Blue Diaper Syndrome

    […] deficiency) Crohn's disease , liver and renal disease Clinical findings : immune dysfunction, impaired wound healing , hypogonadism , diarrhea , dermatitis , alopecia , abnormal[] Jackson C, Buchman AL: Advances in the management of short bowel syndrome. Curr Gastroenterol Rep 2005;7:373–378. Parekh NR, Steiger E: Short bowel syndrome.[] Ten of 102 subjects (9.8%) with fructose malabsorption had zinc deficiency (serum zinc concentration 10.7 μmol/L), whereas in the group with normal fructose absorption, 45[]

  • Hereditary Mucoepithelial Dysplasia

    Congenital alopecia involving the scalp, eyebrows and eyelashes is another essential cutaneous manifestation of IFAP (Figure 1A ).[] Pediatr Radiol 36(3):233–2409 PubMed CrossRef Google Scholar Duro D, Kamin D, Duggan C (2008) Overview of pediatric short bowel syndrome.[] IFAP syndrome is caused by deficiency in MBTPS2, an intramembrane zinc metalloprotease essential for cholesterol homeostasis and ER stress response.[]

  • Laron Syndrome with Immunodeficiency

    bowel syndrome H01602 Gastroesophageal reflux disease H01615 Irritable bowel syndrome H01634 Peptic ulcer H01782 Eosinophilic gastrointestinal disorder H01853 Chronic nonspecific[] alopecia 1 Palmoplantar Keratoderma, Epidermolytic 4 Palmoplantar Keratoderma, Nonepidermolytic 2 Pancreatic agenesis and congenital heart defects 1 Pancreatic Agenesis,[] T-cell immunodeficiency, congenital alopecia, and nail dystrophy 1 0 Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-negative[]

  • Gorlin-Chaudhry-Moss Syndrome

    This infrequent disorder can be precipitated by intake of a large amount of sugars, in patients with short bowel ... 420 Abdominal compartment syndrome - a major complication[] Deficiency due to Low Breast Milk Zinc NEURODEVELOPMENTAL DISORDER WITH SPASTICITY AND POOR GROWTH Neurofaciodigitorenal Syndrome Nijmegen Breakage Syndrome-Like Disorder[] Alopecia 2 Palmoplantar Keratoderma and Congenital Alopecia, Autosomal Dominant Papillon-Lefevre Syndrome Pili Torti and Developmental Delay Pilodental Dysplasia with Refractive[]

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