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Seckel syndrome 4

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Description

Seckel syndrome is a rare autosomal recessive disorder characterized by severe pre- and postnatal growth retardation, severe microcephaly with mental retardation, and specific dysmorphic features (Faivre et al., 2002). For a general description and a discussion of genetic heterogeneity of Seckel syndrome, see 210600.

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

112

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Genes

External Links

  • OMIM

    613676

  • Orphanet
  • HPO
  • Medgen

    C3888212

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