The de Barsy syndrome
We report a child with de Barsy syndrome, which is a very rare, genetically transmitted clinical entity associated with mental and growth retardation, severe cutis laxa, joint laxity and various ocular and skeletal system findings. The patient was operated to treat her orthopedic disabilities...
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| Hlavní autoři: | , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Hacettepe University Institute of Child Health
2001-01-01
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| Edice: | The Turkish Journal of Pediatrics |
| On-line přístup: | https://turkjpediatr.org/article/view/3023 |
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