Open AccessNaegeli–Franceschetti–Jadassohn syndrome: A rare reticulate pigmentary disorder
Author(s) -
Manjunath Hulmani,
Gitika Sanodia,
VJagannath Kumar
Publication year - 2019
Publication title -
indian journal of dermatology
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 0.395
H-Index - 36
eISSN - 1998-3611
pISSN - 0019-5154
DOI - 10.4103/ijd.ijd_653_16
Subject(s) - medicine , dermatology , ectodermal dysplasia , tooth abnormality , nail (fastener) , reticulate , dermatoglyphics , pathology , dentistry , biology , genetics , materials science , botany , metallurgy
Naegeli-Franceschetti-Jadassohn syndrome is a rare autosomal dominant form of ectodermal dysplasia affecting sweat glands, nails, teeth, and skin. We report a case of 16-year-old female who had generalized reticulate pigmentation, dental changes, nail changes, and absence of dermatoglyphics and hypohydrosis.
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