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Pseudoatrophoderma colli

MedGen UID:
96061
•Concept ID:
C0406561
•
Disease or Syndrome
Synonym: Pseudoatrophoderma Colli
SNOMED CT: Pseudoatrophoderma colli (238840009)
 
Monarch Initiative: MONDO:0008325
OMIM®: 177350

Clinical features

From HPO
Abnormality of the skin
MedGen UID:
11449
•Concept ID:
C0037268
•
Congenital Abnormality
An abnormality of the skin.
See: Feature record | Search on this feature

Recent clinical studies

Diagnosis

Pseudoatrophoderma colli. A familial case.
Kauh YC, Knepp ME, Luscombe HA
Arch Dermatol 1980 Oct;116(10):1181-2. PMID: 7425667
Pseudoatrophoderma colli in a male.
Kanan MW, Kandil E
Br J Dermatol 1969 Jan;81(1):65-8. doi: 10.1111/j.1365-2133.1969.tb15921.x. PMID: 5763638
Pseudoatrophoderma colli, acanthosis nigricans, and confluent and reticular papillomatosis.
KESTEN BM, JAMES HD
AMA Arch Derm 1957 Apr;75(4):525-42. doi: 10.1001/archderm.1957.01550160051007. PMID: 13410113

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