Identical Twins with Infantile Systemic Hyalinosis: Case study and review of literature

INTRODUCTION: Infantile Systemic Hyalinosis (ISH) is a rare and fatal genetic disorder with mutations in Capillary morphogenesis gene-2 CMG2 / Human anthrax toxin receptor gene-2 ANTXR2 resulting in spindle cell proliferation, altered collagen metabolism with extensive deposition of amorphous eosino...

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Detalhes bibliográficos
Publicado no:J Orthop Case Reports
Main Authors: Aggarwal, Maheshwar Lakkireddyl Shagun, Chilakamarri, Vijaykrishna, Chennuri, Vasundhara S, Karra, Madhulatha
Formato: Artigo
Idioma:Inglês
Publicado em: Indian Orthopaedic Research Group 2016
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4845419/
https://ncbi.nlm.nih.gov/pubmed/27299133
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.13107/jocr.2250-0685.382
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