Dentistry · Dentistry / Periodontology
Zimmermann–Laband syndrome
also: Gingival fibromatosis with nail dysplasia
Gingival fibromatosis with absent nails and coarse facies.
- Specialty
- Dentistry
- Subspecialty
- Dentistry / Periodontology
- Sex & age distribution
- Male: affected; Female: affected; Children: yes
- Gene(s) involved
- ATP6V1B2, KCNH1, KCNN3
- Alternative names & eponyms
- Gingival fibromatosis with nail dysplasia
Etiology & mechanism
KCNH1 or ATP6V1B2 mutation.
Gene(s) involved (3)
Symptoms & signs (4)
In plain terms, someone with Zimmermann–Laband 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
Hunter syndrome
coarse facies, hepatosplenomegaly
2 shared
Hurler syndrome
coarse facies, hepatosplenomegaly
2 shared
Sly syndrome
coarse facies, hepatosplenomegaly
1 shared
Börjeson–Forssman–Lehmann syndrome
coarse facies
1 shared
Borjeson–Forssman–Lehmann syndrome
coarse facies
1 shared
Cantú syndrome
coarse facies
1 shared
Coffin–Lowry syndrome
coarse facies
1 shared
Coffin–Siris syndrome
coarse facies
1 shared
Costello syndrome
coarse facies
1 shared
Cross syndrome
gingival fibromatosis
Shares genes with
None.
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