OSLAM syndrome

Orpha code: 2760OMIM code: 165660

Definition

A rare genetic disease characterized by the association of osteosarcoma with limb anomalies (such as bilateral radioulnar synostosis and clinodactyly, as well as other abnormalities of the hands and feet) and erythroid macrocytosis without anemia. There have been no further descriptions in the literature since 1977.

Disease data
Classification

Malformation syndrome

Synonyms
Osteosarcoma-limb anomalies-erythroid macrocytosis syndrome
Kostniakomięsak - wady kończyn - makrocytoza krwinek czerwonych
ORPHA code
2760
OMIM code
165660
ICD10 code
C41.9
ICD11 code
-

No additional description.

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