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Cross–McKusick–Breen syndrome (also known as "Cross syndrome", "hypopigmentation and microphthalmia", and "oculocerebral-hypopigmentation syndrome") is an extremely rare disorder characterized by white skin, blond hair with yellow-gray metallic sheen, small eyes with cloudy corneas, jerky nystagmus, and severe intellectual disability and physical retardation. It was characterized in 1967.

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  • Cross syndrome (en)
  • Okulozerebrales Hypopigmentierungs-Syndrom (de)
  • Sindrome di Cross-McKusick-Breen (it)
rdfs:comment
  • Das Okulo-zerebrale Hypopigmentierungs-Syndrom ist ein sehr seltenes angeborenes Krankheitssyndrom bestehend aus Pigmentierungsstörung (Albinismus), Entwicklungshemmung der Augen (Mikrophthalmie) sowie geistiger Entwicklungsverzögerung. Synonyme sind: Cross-McKusick-Breen Syndrom; Cross-Syndrom; Kramer-Syndrom; englisch Depigmentation-Gingival Fibromatosis-Microphthalmia Die Namensbezeichnungen beziehen sich auf den Erstautor bzw. die Autoren der Erstbeschreibung aus dem Jahre 1967 durch H. E. Cross, Victor Almon McKusick und W. Breen sowie auf den Namen der Familie dieser Erstbeschreibung. (de)
  • Cross–McKusick–Breen syndrome (also known as "Cross syndrome", "hypopigmentation and microphthalmia", and "oculocerebral-hypopigmentation syndrome") is an extremely rare disorder characterized by white skin, blond hair with yellow-gray metallic sheen, small eyes with cloudy corneas, jerky nystagmus, and severe intellectual disability and physical retardation. It was characterized in 1967. (en)
  • La sindrome di Cross-McKusick-Breen o sindrome di Kramer è una sindrome a trasmissione autosomica recessiva caratterizzata da ipopigmentazione, difetti oculari e grave ritardo nello sviluppo. (it)
foaf:name
  • Cross syndrome (en)
name
  • Cross syndrome (en)
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  • http://commons.wikimedia.org/wiki/Special:FilePath/Autosomal_recessive_-_en.svg
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ICD
  • E70.3 (en)
OMIM
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  • Cross syndrome is inherited in an autosomal recessive manner (en)
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synonyms
  • Oculocerebral hypopigmentation syndrome, Cross type (en)
has abstract
  • Das Okulo-zerebrale Hypopigmentierungs-Syndrom ist ein sehr seltenes angeborenes Krankheitssyndrom bestehend aus Pigmentierungsstörung (Albinismus), Entwicklungshemmung der Augen (Mikrophthalmie) sowie geistiger Entwicklungsverzögerung. Synonyme sind: Cross-McKusick-Breen Syndrom; Cross-Syndrom; Kramer-Syndrom; englisch Depigmentation-Gingival Fibromatosis-Microphthalmia Die Namensbezeichnungen beziehen sich auf den Erstautor bzw. die Autoren der Erstbeschreibung aus dem Jahre 1967 durch H. E. Cross, Victor Almon McKusick und W. Breen sowie auf den Namen der Familie dieser Erstbeschreibung. (de)
  • Cross–McKusick–Breen syndrome (also known as "Cross syndrome", "hypopigmentation and microphthalmia", and "oculocerebral-hypopigmentation syndrome") is an extremely rare disorder characterized by white skin, blond hair with yellow-gray metallic sheen, small eyes with cloudy corneas, jerky nystagmus, and severe intellectual disability and physical retardation. It was characterized in 1967. (en)
  • La sindrome di Cross-McKusick-Breen o sindrome di Kramer è una sindrome a trasmissione autosomica recessiva caratterizzata da ipopigmentazione, difetti oculari e grave ritardo nello sviluppo. (it)
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ICD10
  • E70.3 (ILDSE70.380)
OMIM id
ORPHA
  • 2719
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