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Ear-patella-short stature syndrome

Orpha number ORPHA2554
Synonym(s) Meier-Gorlin syndrome
Prevalence <1 / 1 000 000
Inheritance
  • Autosomal recessive
Age of onset Neonatal/infancy
ICD-10
  • Q87.1
OMIM
UMLS
  • C1868684
MeSH
  • C538012
MedDRA -
SNOMED CT -

Summary

Ear-patella-short stature syndrome is an association of malformations including bilateral microtia (severe hypoplasia of ear pinnae), absent patellae, short stature, poor weight gain, and characteristic facial features such as high forehead, micrognathism with full lips and small mouth, and accentuated nasolabial folds (smile wrinkles linking the nostrils to the labial commissure). Ear-patella-short stature syndrome is a rare condition, with less than 50 cases reported in the literature. Other skeletal anomalies include dislocation of the elbow, slender ribs and long bones, abnormal modelling of the glenoid fossas with hooked clavicles, and clinodactyly. Bone age is significantly delayed and long bone epiphyses are flattened. Hypoplastic genitalia have been reported in affected boys and girls. Some patients have severe deafness, which may impair neuromotor and mental development, and cognitive ability may be subnormal. The etiology remains unknown: all genes evaluated in affected patients were normal. Reports of parental consanguinity in some cases, the equal sex ratio, and the occurrence of affected sibs provide strong evidence for an autosomal recessive mode of inheritance. Neuroradiographic imaging and functional inner ear investigations are recommended in the diagnostic workup.


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