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Indian J Hum Genet ; 2014 Apr-Jun ; 20 (2): 192-194
Artículo en Inglés | IMSEAR | ID: sea-156660

RESUMEN

Constitutional mismatch repair deficiency syndrome is a rare autosomal recessive syndrome caused by homozygous mutations in mismatch repair genes. This is characterized by the childhood onset of brain tumors, colorectal cancers, cutaneous manifestations of neurofibromatosis‑1 like café au lait spots, hematological malignancies, and occasionally other rare malignancies. Here, we would like to present a family in which the sibling had glioblastoma, and the present case had acute lymphoblastic lymphoma and colorectal cancer. We would like to present this case because of its rarity and would add to literature.


Asunto(s)
Niño , /diagnóstico , Reparación de la Incompatibilidad de ADN/genética , Humanos , Síndrome de Lynch II/diagnóstico , Síndrome de Lynch II/genética , Masculino
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