Hoyeraal-Hreidarsson syndrome
(Q9390252)
a rare multisystem disease characterized by intrauterine growth retardation, microcephaly, cerebellar hypoplasia, progressive combined immune deficiency and aplastic anemia.
a rare multisystem disease characterized by intrauterine growth retardation, microcephaly, cerebellar hypoplasia, progressive combined immune deficiency and aplastic anemia.
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Hoyeraal-Hreidarsson syndrome
other details
aliases |
Progressive pancytopenia-immunodeficiency-cerebellar hypoplasia syndrome |
description | a rare multisystem disease characterized by intrauterine growth retardation, microcephaly, cerebellar hypoplasia, progressive combined immune deficiency and aplastic anemia. |
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