Duchenne muscular dystrophy/rhabdomyosarcoma, ichthyosis vulgaris/acute monoblastic leukemia: Association of rare genetic disorders and childhood malignant diseases

Medical and Pediatric Oncology

Volumn 39, Issue 1, 2002, Pages 66-68

  Jakab, Zsuzsanna ^a   Szegedi, István ^a   Balogh, Erzsébet ^a   Kiss, Csongor ^a   Oláh, Éva ^a,b  

^a UNIVERSITY OF DEBRECEN   (Hungary)

^b UNIVERSITY OF DEBRECEN   (Hungary)

Author keywords

Childhood cancer; Duchenne muscular dystrophy; Genetic disease; Ichthyosis; Leukemia; Rhabdomyosarcoma

Indexed keywords

ALPHA TOCOPHEROL; GLUTAMIC ACID; THIAMINE;

ACUTE MONOCYTIC LEUKEMIA; ARTICLE; BRAIN EDEMA; CASE REPORT; CHILD; CLINICAL FEATURE; DISEASE ASSOCIATION; DISEASE COURSE; DUCHENNE MUSCULAR DYSTROPHY; FAMILY HISTORY; FEMALE; GENETIC ANALYSIS; GENETIC PREDISPOSITION; GENETIC RISK; HUMAN; ICHTHYOSIS VULGARIS; MALE; MOTOR DEVELOPMENT; PHYSIOTHERAPY; PRIORITY JOURNAL; RHABDOMYOSARCOMA;

CHILD; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; FATAL OUTCOME; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; ICHTHYOSIS VULGARIS; ICHTHYOSIS, X-LINKED; LEUKEMIA, LYMPHOCYTIC, ACUTE, L1; MALE; MUSCULAR DYSTROPHY, DUCHENNE; PAROTID GLAND; PAROTID NEOPLASMS; PEDIGREE; RHABDOMYOSARCOMA;

EID: 0036113320     PISSN: 00981532     EISSN: None     Source Type: Journal    
DOI: 10.1002/mpo.10043     Document Type: Article

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