Sporadic Fibrodysplasia Ossificans Progressiva in an Egyptian Infant with c.617G > A Mutation in <i>ACVR1</i> Gene: A Case Report and Review of Literature

<table>Clinical data: (a) pedigree of the family showing no consanguinity and no family history, (b) photographic profile for the baby’s face showing sparse scalp hairs, (c) photograph for the baby’s feet showing marked shortening, sharpening of both big toes, with hallux valgus deformities, and (d) para-vertebral hard swellings more on the left side.</table>

Case Reports in Genetics

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Figure 1: Sporadic Fibrodysplasia Ossificans Progressiva in an Egyptian Infant with c.617G > A Mutation in <i>ACVR1</i> Gene: A Case Report and Review of Literature 

Figure 1 | Sporadic Fibrodysplasia Ossificans Progressiva in an Egyptian Infant with c.617G > A Mutation in ACVR1 Gene: A Case Report and Review of Literature 