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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Detalles Bibliográficos
Autores principales: Aggarwal, Maheshwar Lakkireddyl Shagun, Chilakamarri, Vijaykrishna, Chennuri, Vasundhara S, Karra, Madhulatha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Indian Orthopaedic Research Group 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4845419/
https://www.ncbi.nlm.nih.gov/pubmed/27299133
http://dx.doi.org/10.13107/jocr.2250-0685.382

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4845419/
https://www.ncbi.nlm.nih.gov/pubmed/27299133
http://dx.doi.org/10.13107/jocr.2250-0685.382

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