Cutis Laxa Syndrome: A Rare Genetic Disorder of Elastolysis
DOI:
https://doi.org/10.3329/dshj.v34i1.51831Keywords:
Cutis Laxa Syndrome, ElastolysisAbstract
Abstract not available
DS (Child) H J 2018; 34(1) : 59-62
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Published
2021-02-03
How to Cite
Rahman, M. M., Bhuiyan, A. T., & Islam, M. A. (2021). Cutis Laxa Syndrome: A Rare Genetic Disorder of Elastolysis. Dhaka Shishu (Children) Hospital Journal, 34(1), 59–62. https://doi.org/10.3329/dshj.v34i1.51831
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Case Report