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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...
Autores principales: | Aggarwal, Maheshwar Lakkireddyl Shagun, Chilakamarri, Vijaykrishna, Chennuri, Vasundhara S, Karra, Madhulatha |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Indian Orthopaedic Research Group
2016
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Materias: | |
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 |
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