Infantile genetic agranulocytosis, morbus Kostmann: Presentation of six cases from the original "Kostmann family" and a review

Acta Paediatrica, International Journal of Paediatrics

Volumn 90, Issue 7, 2001, Pages 757-764

  Carlsson, G ^a   Fasth, A ^a  

^a SUNDERBY HOSPITAL   (Sweden)

Author keywords

Agranulocytosis; Autosomal recessive; G CSF treatment; Kostmann

Indexed keywords

RECOMBINANT GRANULOCYTE COLONY STIMULATING FACTOR;

AGRANULOCYTOSIS; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; FATALITY; FEMALE; HOSTMANN SYNDROME; HUMAN; INFANT; KOSTMANN SYNDROME; MALE; PRESCHOOL CHILD; PRIORITY JOURNAL; SURVIVAL; TREATMENT OUTCOME;

ADOLESCENT; ADULT; AGRANULOCYTOSIS; CHILD; CHILD, PRESCHOOL; CHRONIC DISEASE; FEMALE; GRANULOCYTE COLONY-STIMULATING FACTOR; HUMANS; MALE; NEUTROPENIA; PROGNOSIS; QUALITY OF LIFE; SWEDEN; SYNDROME;

EID: 0034899047     PISSN: 08035253     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1651-2227.2001.tb02801.x     Document Type: Article

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