Mowat–Wilson syndrome – case study
Mowat–Wilson syndrome is a rare genetic condition characterised by a number of congenital anomalies, including facial dysmorphia, heart and kidney anomalies, Hirschsprung’s disease, intellectual disability and abnormalities of reproductive organs. In the paper, we present a case of a girl who was...
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| Principais autores: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Medical Communications Sp. z o.o.
2016-06-01
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| Series: | Pediatria i Medycyna Rodzinna |
| Assuntos: | |
| Acceso en liña: | http://www.pimr.pl/index.php/issues/2016-vol-12-no-2/mowat-wilson-syndrome-case-study?aid=958 |
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