Cutaneous ossification is a marker of Albright hereditary osteodystrophy

Cutaneous ossification is a rare group of disorders seen in paediatric population. Initial presentation is with asymptomatic hard lesion in skin. It may manifest at birth or shortly thereafter. In addition to cutaneous manifestation child may have dysmorphic features or stigmata of end organ resistance to hormones. Here we report a case of Albright hereditary osteodystrophy in a four years and seven months old girl for its rarity.