A further case of a Prader-Willi syndrome phenotype in a patient with Angelman syndrome molecular defect
Angelman syndrome (AS) and Prader-Willi syndrome (PWS) are distinct human neurogenetic disorders; however, a clinical overlap between AS and PWS has been identified. We report on a further case of a patient showing the PWS phenotype with the AS molecular defect. Despite the PWS phenotype, the DNA me...
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| Autori principali: | , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Thieme Revinter Publicações
2002-01-01
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| Serie: | Arquivos de Neuro-Psiquiatria |
| Soggetti: | |
| Accesso online: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2002000600024 |
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