A case of hidrotic ectodermal dysplasia with developing eccrine syringofibroadenoma with heterozygous mutation of GJB6 gene
J Dermatol
.
2022 Dec;49(12):e451-e452.
doi: 10.1111/1346-8138.16565.
Epub 2022 Sep 2.
Authors
Akiko Nishibu
1
2
,
Tomoko Iwanaga
1
2
,
Tsuyoshi Ushigami
1
,
Takashi Mochizuki
1
Affiliations
1
Department of Dermatology, Kanazawa Medical University, Uchinada, Japan.
2
Department of Dermatology, Ushitsu General Hospital, Ushitsu, Japan.
PMID:
36052808
DOI:
10.1111/1346-8138.16565
No abstract available
Publication types
Case Reports
Letter
MeSH terms
Connexin 30 / genetics
Ectodermal Dysplasia* / diagnosis
Ectodermal Dysplasia* / genetics
Humans
Mutation
Poroma*
Sweat Gland Neoplasms*
Substances
Connexin 30
GJB6 protein, human