Hyaline Fibromatosis Syndrome [Infantile Systemic Hyalinosis and Juvenile Hyaline Fibromatosis ] – Pathology Infographic

 

Hyaline fibromatosis syndrome is the current name for clinical manifestations of diseases previously known as “infantile systemic hyalinosis” and “juvenile hyaline fibromatosis”.

Infantile systemic hyalinosis and juvenile hyaline fibromatosis are very rare recessive autosomal hereditary diseases that arise from mutation of gene ANTXR2 (anthrax toxin receptor-2), also known as gene CMG2 (capillary morphogenesis gene2), located in chromosome 4q21.

Visit: Pathology of Juvenile Hyaline Fibromatosis

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