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Temple syndrome due to maternal uniparental disomy of chromosome 14

Disease definition

A rare chromosomal anomaly characterized by prenatal and postnatal growth retardation, hypotonia, motor delay, early puberty, obesity, short adult stature, small hands and feet, mild intellectual disability, and mild dysmorphic facial features (frontal bossing, short nose with wide nasal tip, micrognathia, high palate, short philtrum).


Classification level: Subtype of disorder
  • Synonym(s):
    • UPD(14)mat
  • Prevalence: <1 / 1 000 000
  • Inheritance: -
  • Age of onset: Antenatal, Neonatal
  • ICD-10: Q99.8
  • ICD-11: LD2Y
  • OMIM: 616222
  • UMLS: C5680248
  • MeSH: -
  • GARD: -
  • MedDRA: -

Detailed information

General public

Disease review articles

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