Endocrinology · Endocrinology / Diabetes
Mauriac syndrome
also: Glycogenic hepatopathy with growth failure in diabetes
Growth failure, hepatomegaly and delayed puberty in poorly controlled type 1 diabetes.
- Specialty
- Endocrinology
- Subspecialty
- Endocrinology / Diabetes
- Sex & age distribution
- Male: affected; Female: affected; Children: yes, children and adolescents
- Gene(s) involved
- None recorded
- Alternative names & eponyms
- Glycogenic hepatopathy with growth failure in diabetes
Etiology & mechanism
Chronic hyperglycemia with glycogen deposition in liver.
Gene(s) involved (0)
No gene recorded for this syndrome.
Symptoms & signs (6)
In plain terms, someone with Mauriac 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
Aarskog–Scott syndrome
delayed puberty, short stature
2 shared
Pituitary stalk interruption syndrome
delayed puberty, short stature
1 shared
3M syndrome
short stature
1 shared
Andersen–Tawil syndrome
short stature
1 shared
Bloom syndrome
short stature
1 shared
Börjeson–Forssman–Lehmann syndrome
short stature
1 shared
Budd–Chiari syndrome
hepatomegaly
1 shared
Cardio-facio-cutaneous syndrome
short stature
1 shared
Caroli syndrome
hepatomegaly
1 shared
Chanarin–Dorfman syndrome
hepatomegaly
Shares genes with
None.
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