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Results 1 - 10 of 24 for Aplasia cutis congenita of scalp
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  1. Nonsyndromic aplasia cutis congenita 
    ... CONGENITA, NONSYNDROMIC; ACC PubMed Abulezz TA, Shalkamy MA. Aplasia cutis congenita: Two cases of non-scalp lesions. Indian J Plast Surg. 2009 Jul;42( ...
    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 Testing ...
    https://medlineplus.gov/genetics/condition/adams-oliver-syndrome - Genetics
  3. NOTCH1 gene 
    ... a condition characterized by areas of missing skin (aplasia cutis congenita), usually on the scalp, and malformations of the hands and feet. These ...
    https://medlineplus.gov/genetics/gene/notch1 - Genetics
  4. RBPJ gene 
    ... a condition characterized by areas of missing skin (aplasia cutis congenita), usually on the scalp, and malformations of the hands and feet. These ...
    https://medlineplus.gov/genetics/gene/rbpj - Genetics
  5. ARHGAP31 gene 
    ... a condition characterized by areas of missing skin (aplasia cutis congenita), usually on the scalp, and malformations of the hands and feet. These ...
    https://medlineplus.gov/genetics/gene/arhgap31 - Genetics
  6. DOCK6 gene 
    ... a condition characterized by areas of missing skin (aplasia cutis congenita), usually on the scalp, and malformations of the hands and feet. Neurological ...
    https://medlineplus.gov/genetics/gene/dock6 - Genetics
  7. DLL4 gene 
    ... a condition characterized by areas of missing skin (aplasia cutis congenita), usually on the scalp, and malformations of the hands and feet. Some ...
    https://medlineplus.gov/genetics/gene/dll4 - Genetics
  8. EOGT gene 
    ... condition is characterized by areas of missing skin (aplasia cutis congenita), usually on the scalp, and malformations of the hands and feet. The ...
    https://medlineplus.gov/genetics/gene/eogt - Genetics
  9. Scalp-ear-nipple syndrome 
    ... nipple syndrome are born with a condition called aplasia cutis congenita, which involves patchy abnormal areas (lesions) on the scalp. These lesions are firm, raised, hairless nodules that ...
    https://medlineplus.gov/genetics/condition/scalp-ear-nipple-syndrome - Genetics
  10. KCTD1 gene 
    ... of the tissues that arise from the ectoderm (ectodermal dysplasia) and leads to the signs and symptoms of scalp-ear-nipple syndrome. More About This Health Condition ...
    https://medlineplus.gov/genetics/gene/kctd1 - Genetics
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