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Autosomal Recessive Cutis Laxa Type II: Report of Novel Mutation in a Child
Autosomal recessive cutis laxa type-II (ARCLII) is a spectrum of clinical disorders with prenatal and postnatal growth retardation, cutis laxa, dysmorphism, and skeletal abnormalities. We report the case of a 14-month-old boy with developmental delay, hypotonia, dysmorphism, and loose skin. A novel...
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| Publicado no: | Indian Dermatol Online J |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5621197/ https://ncbi.nlm.nih.gov/pubmed/28979870 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/idoj.IDOJ_334_16 |
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