Zunich-Kaye syndrome (Q83138)
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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
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dki-india-ID_920396015
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Concluído
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13 August 2026
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