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Carlsson, G. and Fasth, A. (2001) Infantile Genetic Agranulocytosis, Morbus Kostmann: Presentation of Six Cases from the Original “Kostmann Family” and a Review. Acta Paediatrica, 90, 757-764.
https://doi.org/10.1080/080352501750315663

has been cited by the following article:

• TITLE: Kostmann’s Neutropenia: A Case Report

  AUTHORS: Khaoula Achir, Ilham Tadmori, Mounia Lakhdar Idrissi, Fatima Zahra Souilmi, Mohamed Hbibi, Moustapha Hida

  KEYWORDS: Kostmann Syndrome, Severe Congenital Neutropenia, Skin Abscesses

  JOURNAL NAME: Open Journal of Pediatrics, Vol.14 No.5, September 10, 2024

  ABSTRACT: Kostmann syndrome, or severe congenital neutropenia, is a rare condition in children marked by a neutrophil count of less than 500/mm3. This congenital agranulocytosis, an autosomal recessive genetic disorder, is often first identified by a neonatal infectious syndrome. The deficiency in neutrophils increases susceptibility to bacterial and fungal infections. Prior to the availability of hematopoietic growth factors, the disease was associated with significant morbidity and early mortality. We present the case of a 17-month-old boy who was admitted to the pediatric emergency department at Hassan II University Hospital in Fes with skin abscesses.