Orphanet: Cataract growth hormone deficiency sensory neuropathy sensorineural hearing loss skeletal dysplasia syndrome
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Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome

Disease definition

A rare mitochondrial disease characterized by a highly variable phenotypic spectrum comprising delayed motor development, peripheral neuropathy, cataract, short stature due to growth hormone deficiency, nystagmus, sensorineural hearing loss, dysmorphic facial features, and skeletal abnormalities consistent with spondyloepimetaphyseal dysplasia. Hyperextensible joints, achalasia, and telangiectasia have also been described. Cognition is normal. Atrophy of the pituitary gland has been observed in brain imaging.

ORPHA:436174

Classification level: Disorder
  • Synonym(s):
    • CAGSSS
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal recessive 
  • Age of onset: Infancy, Childhood
  • ICD-10: Q87.8
  • OMIM: 616007
  • UMLS: -
  • MeSH: -
  • GARD: -
  • MedDRA: -
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