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Results 1 - 8 of 8 for aplasia cutis congenita OR "malformation," congenital
Did you mean alaska cutis congenita OR "malformation," congenital?
  1. Nonsyndromic aplasia cutis congenita 
    ... scalp Congenital ulcer of the newborn Scalp defect congenital Genetic Testing Registry: Aplasia cutis congenita Aplasia cutis congenita National Organization for Rare Disorders ( ...
    https://medlineplus.gov/.../nonsyndromic-aplasia-cutis-congenita - Genetics
  2. Adams-Oliver syndrome 
    ... Absence defect of limbs, scalp, and skull AOS Aplasia cutis congenita with terminal transverse limb defects Congenital scalp defects with distal limb reduction anomalies Genetic ...
    https://medlineplus.gov/genetics/condition/adams-oliver-syndrome - Genetics
  3. Skin Conditions (National Library of Medicine)  
    What does your skin do? Your skin is your body's largest organ. It covers the entire outside of your body. There are many ways that your skin protects ...
    https://medlineplus.gov/skinconditions.html - Health Topics
  4. COL7A1 gene 
    ... cause a rare condition called epidermolysis bullosa with congenital localized absence of skin (also known as Bart syndrome or aplasia cutis congenita type VI). Individuals with this condition have patches ...
    https://medlineplus.gov/genetics/gene/col7a1 - Genetics
  5. Pachyonychia congenita 
    Pachyonychia congenita is a condition that primarily affects the skin and nails. The signs and symptoms of this condition usually become apparent within the first ...
    https://medlineplus.gov/genetics/condition/pachyonychia-congenita - Genetics
  6. Epidermolysis bullosa with pyloric atresia 
    Epidermolysis bullosa with pyloric atresia (EB-PA) is a condition that affects the skin and digestive tract. This condition is one of several forms of epidermolysis ...
    https://medlineplus.gov/...pidermolysis-bullosa-with-pyloric-atresia - Genetics
  7. NOTCH1 gene 
    ... a condition characterized by areas of missing skin (aplasia cutis congenita), usually on the scalp, and malformations of the ...
    https://medlineplus.gov/genetics/gene/notch1 - Genetics
  8. Patient support and advocacy groups 
    ... Foundation Dup 15q Alliance Dupuytren Research Group Dyskeratosis Congenita Outreach EA/TEF Child and Family Support Connection ECD Global Alliance Ectodermal Dysplasia Society Ehlers-Danlos Society Ehlers-Danlos Support - UK ...
    https://medlineplus.gov/about/general/genetics/supportadvocacygroups -