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264 Possible Causes for Congenital Alopecia, Short Bowel Syndrome

  • Alopecia

    Congenital triangular alopecia Congenital triangular alopecia references Congenital triangular alopecia Congenital triangular alopecia is a patch of hair loss in the temple[keratin.com] Despite the low prevalence, congenital alopecia areata is an important differential diagnosis for neonatal hair loss.[ncbi.nlm.nih.gov] A breach in this immune privilege state is considered as the cause of alopecia areata. [4] A few cases of babies being born with congenital alopecia areata have been reported[en.wikipedia.org]

  • Alopecia Areata

    We report 4 cases of congenital alopecia areata with follow-up from 3 to 5 years. The diagnosis was made clinically in all cases.[ncbi.nlm.nih.gov] During the first appointment, diagnoses of alopecia areata and congenital triangular alopecia were made. After one year, there was no change.[ncbi.nlm.nih.gov] Despite the low prevalence, congenital alopecia areata is an important differential diagnosis for neonatal hair loss.[ncbi.nlm.nih.gov]

  • Hypothyroidism

    […] of the puppy coat, hyperpigmentation of the skin, and bilaterally symmetric alopecia of the trunk.[web.archive.org] 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[ncbi.nlm.nih.gov] Alopecia, weight gain, mental dullness, fatigue, cold intolerance, infertility and neurological deficits are seen.[medical-dictionary.thefreedictionary.com]

  • Cerebellotrigeminal Dermal Dysplasia

    alopecia of a zone of the occipital and posterior parietal scalp is presented.[ncbi.nlm.nih.gov] bowel syndrome).[sites.uclouvain.be] Bargman H: Congenital temporal triangular alopecia. Can Med Assoc J 1984;131:1253–1254.[karger.com]

  • Zinc Deficiency

    Malnutrition, prematurity, total parenteral nutrition dependence, and burns increase the demand for zinc, whereas congenital malabsorption syndromes represent clinical situations[ncbi.nlm.nih.gov] […] diseases such as ulcerative colitis and Crohn’s disease, and nutrient absorption syndromes such as short bowel syndrome and celiac disease.[doctorshealthpress.com] Gastrointestinal diseases including ulcerative colitis, Crohn's disease, short bowel syndrome and chronic diarrhoea. Chronic liver disease. Chronic kidney disease.[patient.info]

  • Salti-Salem Syndrome

    Kapoor Ramji Syndrome SHASHI-PENA SYNDROME Sheehan syndrome short bowel syndrome short QT syndrome Short Stature-Obesity Syndrome SHORT Syndrome shoulder impingement syndrome[rgd.mcw.edu] Alopecia X-Linked Congenital Infantile Muscular Dystrophy with Cataract and Hypogonadism Cutaneous Telangiectasia and Cancer Syndrome, Familial De Sanctis-Cacchione Syndrome[rgd.mcw.edu] Sho [ edit ] Shock Shokeir syndrome Shor [ edit ] Short b – Short r [ edit ] Short bowel syndrome Short broad great toe macrocranium Short-chain acyl-CoA dehydrogenase deficiency[en.wikipedia.org]

  • 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.[explainmedicine.com] 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[mdedge.com] It is characterized by inflammation of the skin (dermatitis) around bodily openings (periorificial) and the tips of fingers and toes (acral), hair loss (alopecia), and diarrhea[en.wikipedia.org]

  • Tollner-Horst-Manzke Syndrome

    Ramji Syndrome SHASHI-PENA SYNDROME Sheehan syndrome short bowel syndrome short QT syndrome SHORT STATURE, BRACHYDACTYLY, INTELLECTUAL DEVELOPMENTAL DISABILITY, AND SEIZURES[rgd.mcw.edu] alopecia Autosomal dominant partial epilepsy with auditory features Autosomal dominant polycystic kidney disease - Not a rare disease Autosomal dominant pseudohypoaldosteronism[rarediseases.info.nih.gov] Severe Mental Retardation, with Spasticity and Pigmentary Tapetoretinal Degeneration Sezary's disease Shaheen Syndrome Shaken Baby Syndrome Shapiro Syndrome Sharma Kapoor[rgd.mcw.edu]

  • Dilated Cardiomyopathy Type 2B

    , type I 311300 300017 X-linked dominant FLNA Xq28 Heterotopia, periventricular 300049 300017 X-linked dominant FLNA Xq28 Congenital short bowel syndrome 300048 300017 X-linked[mnglabs.com] Alopecia, and Nail Dystrophy TCL016 TIDAND T-Cell Immunodeficiency, Recurrent Infections, and Autoimmunity with or Without Cardiac Malformations TCL021 TIIAC T-Cell Large[malacards.org] , Autosomal Recessive 8 1 Ichthyosis, Congenital, Autosomal Recessive 9 1 Ichthyosis, Congenital, Autosomal Recessive, Nipal4-Related 2 Ichthyosis, Cyclic, With Epidermolytic[preventiongenetics.com]

  • Autosomal Dominant Macrothrombocytopenia

    , Autosomal Recessive 8 1 Ichthyosis, Congenital, Autosomal Recessive 9 1 Ichthyosis, Congenital, Autosomal Recessive, Nipal4-Related 2 Ichthyosis, Cyclic, With Epidermolytic[preventiongenetics.com] Congenital dyserythropoietic anemia type I Congenital short bowel syndrome Congenital valvular dysplasia Desmoid tumor Early-onset autosomal dominant Alzheimer disease Ehlers-Danlos[csbg.cnb.csic.es] Hyperkeratosis 2 Ichthyosis, Leukocyte Vacuoles, Alopecia, And Sclerosing Cholangitis 2 Idiopathic Fibrosing Alveolitis, Chronic Form 3 Idiopathic Hypercalcemia Of Infancy[preventiongenetics.com]

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