Sjogren–Larsson Syndrome: A Familial Disease Afflicting Three Siblings Born of a Nonconsanguinous Marriage
Sjogren-Larsson syndrome (SLS) is an autosomal recessive ichthyotic syndrome characterized by a triad of congenital ichthyosis, mental retardation, and diplegia or tetraplegia. It occurs due to the defect in the gene responsible for encoding the enzyme fatty aldehyde dehydrogenase. Accumulating thes...
محفوظ في:
| المؤلفون الرئيسيون: | , , , |
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| التنسيق: | Artigo |
| اللغة: | Inglês |
| منشور في: |
Wolters Kluwer Medknow Publications
2024-12-01
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| سلاسل: | Indian Journal of Paediatric Dermatology |
| الموضوعات: | |
| الوصول للمادة أونلاين: | https://journals.lww.com/10.4103/ijpd.ijpd_116_24 |
| الوسوم: |
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