Sindrome de Pallister Killian ou tetrassomia do braco curto do cromossomo 12 em mosaico : relato de dois casos diagnosticados pela hibridizacao in situ por fluorescencia (FISH)

Sugayama, Sofia Mizuho; Bertola, Debora Romeu; Albano, Lilian Maria Jose; Manissadjian, Antranik; Bittencourt, Eloisa Auler; Borovik, Cleide; Chong, Ae Kim

Sindrome de Pallister Killian ou tetrassomia do braco curto do cromossomo 12 em mosaico : relato de dois casos diagnosticados pela hibridizacao in situ por fluorescencia (FISH) / Pallister Killian syndrome or tetrasomy of the short arm of the chromosome 12 mosaicism : report on two cases diagnosed by fluorescense in situ hybridization

Sugayama, Sofia Mizuho; Bertola, Debora Romeu; Albano, Lilian Maria Jose; Manissadjian, Antranik; Bittencourt, Eloisa Auler; Borovik, Cleide; Chong, Ae Kim.

Affiliation

Sugayama, Sofia Mizuho; s.af
Bertola, Debora Romeu; s.af
Albano, Lilian Maria Jose; s.af
Manissadjian, Antranik; s.af
Bittencourt, Eloisa Auler; s.af
Borovik, Cleide; s.af
Chong, Ae Kim; s.af

Pediatria (Säo Paulo) ; 22(3): 255-63, 2000. ilus

Article de Pt | LILACS | ID: lil-296475

Bibliothèque responsable: BR66.1

RESUMO

RESUMO

A sindrome de Pallister Killian (SPK) e uma doenca rara caracterizada por multiplas malformacoes, retardo mental profundo e presenca de um isocromossomo...

Sujet(s)

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Indice: LILACS Sujet Principal: Aberrations des chromosomes / Hybridation in situ / Fluorescéine Type d'étude: Diagnostic_studies Limites du sujet: Child / Female / Humans / Male langue: Pt Texte intégral: Pediatria (Säo Paulo) Thème du journal: PEDIATRIA Année: 2000 Type: Article

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