Severe congenital neutropenia
Severe congenital neutropenia (SCN), also often known as Kostmann syndrome or disease, is a group of rare disorders that affect myelopoiesis, causing a congenital form of neutropenia, usually without other physical malformations. SCN manifests in infancy with life-threatening bacterial infections. Kostmann disease (SCN3), the initial subtype recognized, was clinically described in 1956. This type has an autosomal recessive inheritance pattern, whereas the most common subtype, SCN1, shows autosomal dominant inheritance.
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Acute lymphoblastic leukemiaAgranulocytosis infantilis hereditariaCongenital NeutropeniaCyclic neutropeniaG6PC3Granulocyte colony-stimulating factor receptorHAX1Infantile genetic agranulocytosisKostmann's diseaseKostmann diseaseKostmann syndromeList of conditions treated with hematopoietic stem cell transplantationList of diseases (K)List of periodontal diseasesList of primary immunodeficienciesList of syndromesNeutropeniaNeutrophil elastasePeriodontitis as a manifestation of systemic diseaseSCNSevere Congenital NeutropeniaWhite blood cell
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Severe congenital neutropenia
Severe congenital neutropenia (SCN), also often known as Kostmann syndrome or disease, is a group of rare disorders that affect myelopoiesis, causing a congenital form of neutropenia, usually without other physical malformations. SCN manifests in infancy with life-threatening bacterial infections. Kostmann disease (SCN3), the initial subtype recognized, was clinically described in 1956. This type has an autosomal recessive inheritance pattern, whereas the most common subtype, SCN1, shows autosomal dominant inheritance.
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Choroba Kostmanna (zespół Kost ...... pisał (1909-1982) w 1956 roku.
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El síndrome de Kostmann, o neu ...... frente al posible trasplante.
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Kostmanns sjukdom är en sjukdo ...... svenske läkaren på 1940-talet.
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La sindrome di Kostmann è una ...... e la gravità delle infezioni.
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Severe congenital neutropenia ...... utosomal dominant inheritance.
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نقص العدلات الخلقي الشديد «إس ...... ن 1» وفق نمط وراثي جسمي مسيطر.
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DiseasesDB
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ped
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eMedicine topic
1260
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medical diagnosis
medication
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1,004,390,239
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causes
Mutation in genes, depending on type
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ped
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Severe congenital neutropenia
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Infancy
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synonyms
Kostmann disease, Kostmann's a ...... infantile genetic neutropenia
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types
SCN1-SCN5, SCNX
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Choroba Kostmanna (zespół Kost ...... pisał (1909-1982) w 1956 roku.
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El síndrome de Kostmann, o neu ...... o la aparición de infecciones.
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Kostmanns sjukdom är en sjukdo ...... svenske läkaren på 1940-talet.
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La sindrome di Kostmann è una ...... e la gravità delle infezioni.
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Severe congenital neutropenia ...... utosomal dominant inheritance.
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نقص العدلات الخلقي الشديد «إس ...... ن 1» وفق نمط وراثي جسمي مسيطر.
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Choroba Kostmanna
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Kostmann-Syndrom
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Kostmanns sjukdom
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Severe congenital neutropenia
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Sindrome di Kostmann
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Síndrome de Kostmann
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نقص العدلات الخلقي الشديد
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Severe congenital neutropenia
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