Literature DB >> 31413057

Metaphyseal dysplasia, Spahr type: a mimicker of rickets.

Muthuvel Balasubramaniyan1, Anupriya Kaur1, Anindita Sinha2, Nirmal Raj Gopinathan3.   

Abstract

Metaphyseal dysplasias are a heterogeneous group of skeletal dysplasias characterised by metaphyseal irregularities. Due to the presence of metaphyseal changes accompanied with bowing deformity of lower limb, they are likely to be mistaken for rickets. We present a case of a 7-year-old boy, finally diagnosed with metaphyseal dysplasia, Spahr type (MDST) (OMIM # 250400) after his exome sequencing revealed novel variations in the MMP13 gene (OMIM * 600108). This is a rare skeletal dysplasia with only a few cases reported in literature. A compilation of the presentation of the reported cases is given to help the reader understand this rare disorder. To the best of our knowledge, this case of MDST is the first to be reported from India. © BMJ Publishing Group Limited 2019. No commercial re-use. See rights and permissions. Published by BMJ.

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Keywords:  genetics; orthopaedics

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Year:  2019        PMID: 31413057      PMCID: PMC6700560          DOI: 10.1136/bcr-2019-230257

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  1 in total

1.  Special manifestations and treatment of rare cases of snoring with special facial features and hearing loss in children.

Authors:  Jiali Wu; Xiaoli Li; Shumei Chen
Journal:  J Int Med Res       Date:  2022-07       Impact factor: 1.573

  1 in total

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