Retinoblastoma metastatic to the ovary in a patient with Waardenburg syndrome

American Journal of Ophthalmology

Volumn 133, Issue 5, 2002, Pages 716-718

  Moshfeghi, Darius M ^a   Wilson, Matthew W ^a,b   Haik, Barrett G ^a,b   Hill, D Ashley ^b   Rodriguez Galindo, Carlos ^a,b   Pratt, Charles B ^b  

^a UNIVERSITY OF TENNESSEE HEALTH SCIENCE CENTER   (United States)

^b ST JUDE CHILDREN S RESEARCH HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANTINEOPLASTIC AGENT;

ARTICLE; BACKACHE; BONE MARROW METASTASIS; BONE MARROW TRANSPLANTATION; BRAIN METASTASIS; CANCER CHEMOTHERAPY; CANCER DIAGNOSIS; CANCER MORTALITY; CANCER RADIOTHERAPY; CASE REPORT; CLINICAL FEATURE; DISEASE COURSE; ENUCLEATION; FEMALE; HUMAN; HUMERUS; LAPAROTOMY; LEUKOKORIA; OVARY METASTASIS; PRESCHOOL CHILD; PRIORITY JOURNAL; RETINOBLASTOMA; TIBIA; URINE RETENTION; WAARDENBURG SYNDROME;

EID: 0036253159     PISSN: 00029394     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9394(02)01352-1     Document Type: Article

References (5)

1. The incidence of retinoblastoma
2. Successful treatment of metastatic retinoblastoma
3. A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair with congenital deafness
4. A gene for Waardenburg syndrome type 2 maps close to the human homologue of the microphthalmia gene at chromosome 3p12-p14.1
5. Bilateral bicolored irides with Hirschsprung's disease. Neural crest syndrome