Zunich-Kaye syndrome (Q83138)

From determinar.ia.br - Determine suas informações
Zunich-Kaye syndrome is characterised by early-onset migratory ichthyosiform dermatosis, bilateral ocular coloboma, conductive hearing loss, seizures, intellectual deficit, and characteristic facial features: brachycephaly, mild upslanting of the palpebral fissures, pale blue irides, hypertelorism, flat midface and philtrum, anteverted nostrils, thin upper lip and excessive creases around a wide mouth. The acronym CHIME was proposed for the Zunich-Kaye syndrome: Colobomas of the eye, Heart defects, Ichthyosiform dermatosis, Mental retardation, and Ear defects or Epilepsy.
Language Label Description Also known as
default for all languages
ID_920396015
    English
    Zunich-Kaye syndrome
    Zunich-Kaye syndrome is characterised by early-onset migratory ichthyosiform dermatosis, bilateral ocular coloboma, conductive hearing loss, seizures, intellectual deficit, and characteristic facial features: brachycephaly, mild upslanting of the palpebral fissures, pale blue irides, hypertelorism, flat midface and philtrum, anteverted nostrils, thin upper lip and excessive creases around a wide mouth. The acronym CHIME was proposed for the Zunich-Kaye syndrome: Colobomas of the eye, Heart defects, Ichthyosiform dermatosis, Mental retardation, and Ear defects or Epilepsy.

      Statements

      CID11:ID_920396015
      0 references
      dki-india-ID_920396015
      0 references
      Concluído
      0 references
      13 August 2026
      0 references