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Spondyloepimetaphyseal dysplasia, Bieganski type

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Description

X-linked spondyloepimetaphyseal dysplasia with hypomyelinating leukodystrophy (SEMDHL) is an X-linked recessive developmental disorder characterized by slowly progressive skeletal and neurologic abnormalities, including short stature, large and deformed joints, significant motor impairment, visual defects, and sometimes cognitive deficits. Affected individuals typically have normal early development in the first year or so of life, followed by development regression and the development of symptoms. Brain imaging shows white matter abnormalities consistent with hypomyelinating leukodystrophy (summary by Miyake et al., 2017).

OMIM

  • Mode of Inheritance

  • X-linked recessive inheritance

VARIANTS

7

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Genes

External Links

  • OMIM

    300232

  • Orphanet
  • HPO
  • Medgen

    C1846148

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