Dermatology · Dermatology / Genodermatoses
Naegeli–Franceschetti–Jadassohn syndrome
also: Dermatopathia pigmentosa reticularis
Reticulate pigmentation with hypohidrosis and keratoderma.
- Specialty
- Dermatology
- Subspecialty
- Dermatology / Genodermatoses
- Sex & age distribution
- Male: affected; Female: affected, equal; Children: yes, pigmentation from age 2 onwards
- Gene(s) involved
- KRT14
- Alternative names & eponyms
- Dermatopathia pigmentosa reticularis
Etiology & mechanism
Keratin 14 defects affecting basal keratinocyte function.
Gene(s) involved (1)
Symptoms & signs (6)
In plain terms, someone with Naegeli–Franceschetti–Jadassohn syndrome may experience the following — click any to explore related syndromes:
Same gene(s)
Other syndromes that involve one of this syndrome's genes.
Overlapping symptoms
Other syndromes that share symptoms with this one.
Drag nodes, scroll to zoom, click a node to open that syndrome.
Shares symptoms with
2 shared
Olmsted syndrome
nail dystrophy, palmoplantar keratoderma
2 shared
Rapp–Hodgkin syndrome
hypohidrosis, nail dystrophy
1 shared
Bazex syndrome
nail dystrophy
1 shared
Bazex–Dupré–Christol syndrome
hypohidrosis
1 shared
Dyskeratosis congenita
nail dystrophy
1 shared
Ectrodactyly–ectodermal dysplasia–clefting syndrome
hypohidrosis
1 shared
Hallermann–Streiff syndrome
dental anomalies
1 shared
Hay–Wells syndrome
nail dystrophy
1 shared
Hypohidrotic ectodermal dysplasia
hypohidrosis
1 shared
KID syndrome
palmoplantar keratoderma
Shares genes with
None.
Loading…
Loading…