Cohen syndrome (Q1107087)

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Cohen syndrome (CS) is a rare genetic developmental disorder characterized by microcephaly, characteristic facial features, hypotonia, non-progressive intellectual deficit, myopia and retinal dystrophy, neutropenia and truncal obesity
  • COHEN SYNDROME
  • Pepper Syndrome
  • COH1
  • Chs1
  • Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness
  • COHEN SYNDROME; COH1
  • Coh
  • Chs1, Formerly
  • Hypotonia, Obesity, and Prominent Incisors
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English
Cohen syndrome
Cohen syndrome (CS) is a rare genetic developmental disorder characterized by microcephaly, characteristic facial features, hypotonia, non-progressive intellectual deficit, myopia and retinal dystrophy, neutropenia and truncal obesity
  • COHEN SYNDROME
  • Pepper Syndrome
  • COH1
  • Chs1
  • Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness
  • COHEN SYNDROME; COH1
  • Coh
  • Chs1, Formerly
  • Hypotonia, Obesity, and Prominent Incisors

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