Endocrinology · Endocrinology / Pediatric endocrinology
Temple syndrome
also: Maternal UPD14 syndrome
Imprinting disorder with growth restriction and early puberty.
- Specialty
- Endocrinology
- Subspecialty
- Endocrinology / Pediatric endocrinology
- Sex & age distribution
- Male: affected; Female: affected equally; Children: yes
- Gene(s) involved
- DLK1, MEG3
- Alternative names & eponyms
- Maternal UPD14 syndrome
Etiology & mechanism
Maternal UPD14 or paternal deletion.
Gene(s) involved (2)
Symptoms & signs (6)
In plain terms, someone with Temple 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
Cardio-facio-cutaneous syndrome
feeding problems, short stature
2 shared
Cohen syndrome
hypotonia, truncal obesity
2 shared
Kabuki syndrome
feeding problems, hypotonia
2 shared
Lowe syndrome
hypotonia, short stature
2 shared
Marinesco–Sjögren syndrome
hypotonia, short stature
2 shared
Rubinstein–Taybi syndrome
feeding problems, short stature
1 shared
3M syndrome
short stature
1 shared
Aarskog–Scott syndrome
short stature
1 shared
Allan–Herndon–Dudley syndrome
hypotonia
1 shared
Andersen–Tawil syndrome
short stature
Shares genes with
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