Hoyeraal-Hreidarsson syndrome (Q9390252)
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a rare multisystem disease characterized by intrauterine growth retardation, microcephaly, cerebellar hypoplasia, progressive combined immune deficiency and aplastic anemia.
- Progressive pancytopenia-immunodeficiency-cerebellar hypoplasia syndrome
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Hoyeraal-Hreidarsson syndrome |
a rare multisystem disease characterized by intrauterine growth retardation, microcephaly, cerebellar hypoplasia, progressive combined immune deficiency and aplastic anemia. |
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Statements
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Identifiers
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Sitelinks
Wikipedia(5 entries)
- enwiki Hoyeraal–Hreidarsson syndrome
- eswiki Síndrome de Hoyeraal-Hreidarsson
- fiwiki Hoyeraal–Hreidarssonin oireyhtymä
- plwiki Zespół Høyeraala-Hreiðarssona
- trwiki Zinsser-Cole-Engman sendromu