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Lenz-Majewski syndrome: Report of a case with novel mutation in PTDSS1 gene
Parag M Tamhankar1, Lakshmi Vasudevan1, Vandana Bansal2
1Genetic Research Center, National Institute for Research in Reproductive Health, JM Street, Parel, Mumbai, India.
Abstract:
Lenz-Majewski syndrome (LMS) is an extremely rare syndrome characterized by osteosclerosis, intellectual disability, characteristic facies and distinct craniofacial, dental, cutaneous and distal - limb anomalies. Recently, mutations in PTDSS1 gene have been identified as causative in six unrelated individuals. We report the seventh mutation proven case of LMS and provide a concise review of all known patients till date.
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