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Hajdu-Cheney syndrome

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Description

Hajdu-Cheney syndrome (HJCYS) is a rare autosomal dominant skeletal disorder characterized by short stature, coarse and dysmorphic facies, bowing of the long bones, and vertebral anomalies. Facial features include hypertelorism, bushy eyebrows, micrognathia, small mouth with dental anomalies, low-set ears, and short neck. There is progressive focal bone destruction, including acroosteolysis and generalized osteoporosis. Additional and variable features include hearing loss, renal cysts, and cardiovascular anomalies (summary by Ramos et al., 1998; Simpson et al., 2011; Isidor et al., 2011).

OMIM

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

164

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Genes

External Links

  • OMIM

    102500

  • Orphanet

    955

  • HPO
  • Medgen

    C0917715

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