Naegeli–Franceschetti–Jadassohn syndrome: A rare reticulate pigmentary disorder

Naegeli–Franceschetti–Jadassohn syndrome: A rare reticulate pigmentary disorder

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 hypo...

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Main Authors: Gitika Sanodia, Manjunath Hulmani, V Jagannath Kumar
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2019-01-01
Series:Indian Journal of Dermatology
Subjects:
Dermatoglyphics
ectodermal dysplasia
KRT 14 gene
Naegeli–Franceschetti–Jadassohn syndrome
reticulate pigmentation
Online Access:http://www.e-ijd.org/article.asp?issn=0019-5154;year=2019;volume=64;issue=3;spage=235;epage=238;aulast=Sanodia
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spelling doaj-08e99aa94e8e4972b7b97fd05e6e11e82020-11-24T21:28:53ZengWolters Kluwer Medknow PublicationsIndian Journal of Dermatology0019-51541998-36112019-01-0164323523810.4103/ijd.IJD_653_16Naegeli–Franceschetti–Jadassohn syndrome: A rare reticulate pigmentary disorderGitika SanodiaManjunath HulmaniV Jagannath KumarNaegeli–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.http://www.e-ijd.org/article.asp?issn=0019-5154;year=2019;volume=64;issue=3;spage=235;epage=238;aulast=SanodiaDermatoglyphicsectodermal dysplasiaKRT 14 geneNaegeli–Franceschetti–Jadassohn syndromereticulate pigmentation
collection DOAJ
language English
format Article
sources DOAJ
author Gitika Sanodia
Manjunath Hulmani
V Jagannath Kumar
spellingShingle Gitika Sanodia
Manjunath Hulmani
V Jagannath Kumar
Naegeli–Franceschetti–Jadassohn syndrome: A rare reticulate pigmentary disorder
Indian Journal of Dermatology
Dermatoglyphics
ectodermal dysplasia
KRT 14 gene
Naegeli–Franceschetti–Jadassohn syndrome
reticulate pigmentation
author_facet Gitika Sanodia
Manjunath Hulmani
V Jagannath Kumar
author_sort Gitika Sanodia
title Naegeli–Franceschetti–Jadassohn syndrome: A rare reticulate pigmentary disorder
title_short Naegeli–Franceschetti–Jadassohn syndrome: A rare reticulate pigmentary disorder
title_full Naegeli–Franceschetti–Jadassohn syndrome: A rare reticulate pigmentary disorder
title_fullStr Naegeli–Franceschetti–Jadassohn syndrome: A rare reticulate pigmentary disorder
title_full_unstemmed Naegeli–Franceschetti–Jadassohn syndrome: A rare reticulate pigmentary disorder
title_sort naegeli–franceschetti–jadassohn syndrome: a rare reticulate pigmentary disorder
publisher Wolters Kluwer Medknow Publications
series Indian Journal of Dermatology
issn 0019-5154
1998-3611
publishDate 2019-01-01
description 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.
topic Dermatoglyphics
ectodermal dysplasia
KRT 14 gene
Naegeli–Franceschetti–Jadassohn syndrome
reticulate pigmentation
url http://www.e-ijd.org/article.asp?issn=0019-5154;year=2019;volume=64;issue=3;spage=235;epage=238;aulast=Sanodia
work_keys_str_mv AT gitikasanodia naegelifranceschettijadassohnsyndromeararereticulatepigmentarydisorder
AT manjunathhulmani naegelifranceschettijadassohnsyndromeararereticulatepigmentarydisorder
AT vjagannathkumar naegelifranceschettijadassohnsyndromeararereticulatepigmentarydisorder
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