Also called congenital neutropenia, genetic infantile agranulocytosis, Kostmann disease, Kostmann neutropenia, and Kostmann syndrome.
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Congenital or chronic neutropenias: This group includes Kostmann syndrome, which is a severe neutropenia apparent in babies by age 3 months, with the child experiencing recurrent bacterial infections.
If your child has certain genetic syndromes, including Fanconi anemia, Bloom syndrome, Kostmann syndrome, and Down syndrome, he may be at a higher risk of developing AML than other children.
Noonan syndrome (particularly JMML development).
Severe congenital neutropenia (Kostmann syndrome).
Diamond-Blackfan anemia.
Familial platelet disorder with a propensity to develop AML.
Congenital amegakaryocytic thrombocytopenia.
Kluver-Bucy syndrome
Kniest syndrome
Kocher-Debre-Semelaigne syndrome
Koenig's syndrome
Koerber-Salus-Elschnig syndrome
Kohlmeier-Degos syndrome
Korsakoff's syndrome
Kostmann syndrome
Kuskokwim syndrome ...
 See also: Cancer, Infections, Stress, Leukemia, Immune System
  
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