Dermatology · Dermatology / Genodermatoses
Sjögren–Larsson syndrome
also: Fatty aldehyde dehydrogenase deficiency
Congenital ichthyosis with spastic diplegia and intellectual disability.
- Specialty
- Dermatology
- Subspecialty
- Dermatology / Genodermatoses
- Sex & age distribution
- Male: affected; Female: affected, equal; Children: yes, from birth
- Gene(s) involved
- ALDH3A2
- Alternative names & eponyms
- Fatty aldehyde dehydrogenase deficiency
Etiology & mechanism
Fatty aldehyde dehydrogenase deficiency causing lipid accumulation.
Gene(s) involved (1)
Symptoms & signs (7)
In plain terms, someone with Sjögren–Larsson 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
Borjeson–Forssman–Lehmann syndrome
intellectual disability, seizures
2 shared
Cardiofaciocutaneous syndrome
intellectual disability, seizures
2 shared
Crigler–Najjar syndrome
intellectual disability, seizures
2 shared
EAST syndrome
intellectual disability, seizures
2 shared
Mowat–Wilson syndrome
intellectual disability, seizures
2 shared
Sanjad–Sakati syndrome
intellectual disability, seizures
2 shared
Wolf–Hirschhorn syndrome
intellectual disability, seizures
1 shared
Action myoclonus–renal failure syndrome
seizures
1 shared
Adie tonic pupil syndrome
photophobia
1 shared
Alagille syndrome
pruritus
Shares genes with
None.
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