Rhabdomyosarcoma in Roberts syndrome

Rhabdomyosarcoma in Roberts syndrome

A 23-month-old child diagnosed as having Roberts syndrome, born to consanguineous parents, developed a sarcoma botryoides. Cytogenetic evaluation of peripheral blood lymphocytes and tumor cells showed premature centromere separation, which is characteristic of Roberts syndrome.

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Bibliographische Detailangaben
Veröffentlicht in:Cancer genetics and cytogenetics 1988-04, Vol.31 (2), p.285-289
Hauptverfasser: Wenger, Sharon L., Blatt, Julie, Steele, Mark W., Lloyd, David A., Bellinger, Mark, Phebus, Carol K., Horn, Marianna, Jaffe, Ronald
Format: Artikel
Sprache:eng
Schlagworte:
Abnormalities, Multiple
Biological and medical sciences
Child, Preschool
Complex syndromes
Female
Humans
Karyotyping
Medical genetics
Medical sciences
Rhabdomyosarcoma - complications
Rhabdomyosarcoma - genetics
Rhabdomyosarcoma - pathology
Syndrome
Urinary Bladder Neoplasms - complications
Urinary Bladder Neoplasms - genetics
Urinary Bladder Neoplasms - pathology
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Beschreibung
Zusammenfassung:A 23-month-old child diagnosed as having Roberts syndrome, born to consanguineous parents, developed a sarcoma botryoides. Cytogenetic evaluation of peripheral blood lymphocytes and tumor cells showed premature centromere separation, which is characteristic of Roberts syndrome.
ISSN:0165-4608
1873-4456
DOI:10.1016/0165-4608(88)90230-0