Description

Monosomy 7 may be found in a range of conditions, some familial and some sporadic.


Familial occurrence:

(1) familial monosomy 7

(2) cerebellar ataxia/atrophy-pancytopenia syndrome

(3) familial platelet disorder with propensity to AML

 

Sporadic occurrence:

(1) myelodysplasia

(2) myeloproliferative disorder

(3) acute myeloid leukemia

(4) aplastic anemia

(5) juvenile myelomonocytic leukemia

(6) neurofibromatosis type 1

(7) Noonan syndrome

(8) Bloom syndrome

(9) Paroxysmal Nocturnal Hemoglobinuria (PNH)

(10) dyskeratosis congenita

(11) Fanconi anemia

(12) Shwachman-Diamond syndrome


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