Endocrinology · Endocrinology / Diabetes
Wolcott–Rallison syndrome
also: Neonatal diabetes with epiphyseal dysplasia
Neonatal diabetes, skeletal dysplasia and liver failure.
- Specialty
- Endocrinology
- Subspecialty
- Endocrinology / Diabetes
- Sex & age distribution
- Male: affected; Female: affected equally; Children: yes, infancy
- Gene(s) involved
- EIF2AK3
- Alternative names & eponyms
- Neonatal diabetes with epiphyseal dysplasia
Etiology & mechanism
EIF2AK3 loss causes ER stress.
Gene(s) involved (1)
Symptoms & signs (5)
In plain terms, someone with Wolcott–Rallison 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
1 shared
CHARGE syndrome
growth retardation
1 shared
Immunodysregulation polyendocrinopathy enteropathy X-linked syndrome
neonatal diabetes
1 shared
IPEX syndrome
neonatal diabetes
1 shared
Jacobsen syndrome
growth retardation
1 shared
Nijmegen breakage syndrome
growth retardation
1 shared
Noonan syndrome with multiple lentigines
growth retardation
1 shared
Revesz syndrome
growth retardation
1 shared
Trisomy 9 mosaic syndrome
growth retardation
1 shared
Upshaw–Schulman syndrome
renal impairment
1 shared
Warfarin embryopathy syndrome
growth retardation
Shares genes with
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