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A case of a Jordanian male twin with Cohen's syndrome, with genetic analysis and muscle biopsy; case report
INTRODUCTION AND IMPORTANCE: Cohen's syndrome is a rare autosomal recessive developmental disorder. It usually presents with a wide variety of muscular, neurological and ophthalmological clinical features. In this report, we present a rare case of the first Jordanian male identical twin with Co...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8606835/ https://www.ncbi.nlm.nih.gov/pubmed/34840762 http://dx.doi.org/10.1016/j.amsu.2021.103014 |