Naegeli syndrome

(redirected from Franceschetti-Jadassohn syndrome)

Nae·ge·li syn·drome

(nā'gĕ-lē), [MIM*161000]
reticular skin pigmentation, diminished sweating, hypodontia, hyperkeratosis of the palms and soles, and blistering; may be confused with incontinentia pigmenti but is as common in males as in females; autosomal dominant inheritance.
Synonym(s): Franceschetti-Jadassohn syndrome

Nae·ge·li syn·drome

(nā'gĕ-lē sin'drōm)
Reticular skin pigmentation, diminished sweating, hypodontia, and hyperkeratosis of the palms and soles.

Naegeli,

Oskar, Swiss physician, 1885-1959.
Naegeli syndrome - reticular skin pigmentation, diminished sweating, hypodontia, and hyperkeratosis of the palms and soles. Synonym(s): Franceschetti-Jadassohn syndrome
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References in periodicals archive ?
The differential diagnoses of generalized RPD are dyschromatosis universalis hereditaria (DUH), dermatopathia pigmentosa reticularis (DPR), Naegeli- Franceschetti-Jadassohn syndrome and dyskeratosis congenita (DKC).1,2,3 DUH was first described in 1929 by Toyamo,4a rare clinically heterogeneous genodermatosis characterized by both hyper and hypopigmented macules forming a reticulate pattern.1
Naegeli Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: two allelic ectodermal dysplasias caused by dominant mutations in KRT14.
Rare case report of dyschromatosis universalis he-reditaria
A diagnosis of dermatopathia pigmentosa reticularis (DPR) with a differential of Naegeli- Franceschetti-Jadassohn syndrome (NFJS) was made.
Dermatopathia pigmentosa reticularis and atopic dermatitis: A case report of two siblings

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