Kostmann syndrome

Kostmann disease, which is SCN3, is inherited in an autosomal recessive pattern.

Kostmann syndrome is a group of diseases that affect myelopoiesis, causing a congenital form of neutropenia (severe congenital neutropenia [SCN]), usually without other physical malformations. SCN manifests in infancy with life-threatening bacterial infections.

单词	Congenital Neutropenia
释义	Congenital Neutropenia 英语百科 Kostmann syndrome Kostmann syndrome is a group of diseases that affect myelopoiesis, causing a congenital form of neutropenia (severe congenital neutropenia [SCN]), usually without other physical malformations. SCN manifests in infancy with life-threatening bacterial infections.
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Congenital Neutropenia

Kostmann syndrome