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Arthrogryposis (Ophthalmoplegia Retinopathy)
DefinitionDefinition of Arthrogryposis (Ophthalmoplegia Retinopathy) Arthrogryposis multiplex congenita is a heterogeneous condition and many different types are clinically recognisable. Recently, a new type of autosomal dominant arthrogryposis was described in a father and son. We report on a male patient with similar clinical features, confirming this distinct type of arthrogryposis. The condition is characterised by congenital contractures of the hands and feet with diminished or absent phalangeal creases, ophthalmoplegia, a rigid trunk, deep set eyes, and (in the oldest patient) an abnormal electroretinogram. Differential diagnosis from amyoplasia, the different types of distal arthrogryposis, and symphalangism is discussed. SymptomsSymptoms of Arthrogryposis (Ophthalmoplegia Retinopathy) The list of signs and symptoms for Arthrogryposis (Ophthalmoplegia Retinopathy) listed below:
CausesCauses of Arthrogryposis (Ophthalmoplegia Retinopathy) The causes of Arthrogryposis (Ophthalmoplegia Retinopathy) listed below:
DiagnosisDiagnosis of Arthrogryposis (Ophthalmoplegia Retinopathy) Home medical testing related to Arthrogryposis - ophthalmoplegia - retinopathy:
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