Schwartz syndrome

Schwartz syn·drome

(shwōrts), [MIM*255800]

a congenital disorder characterized by myotonic myopathy, dystrophy of epiphyseal cartilages resulting in dwarfism, joint contractures, blepharophimosis, and characteristic facies; autosomal recessive inheritance.

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Schwartz syn·drome

(shwōrts), [MIM*255800]

a congenital disorder characterized by myotonic myopathy, dystrophy of epiphyseal cartilages resulting in dwarfism, joint contractures, blepharophimosis, and characteristic facies; autosomal recessive inheritance.

Farlex Partner Medical Dictionary © Farlex 2012

Schwartz,

Oscar, U.S. pediatrician, 1919–.

Schwartz syndrome - multiple congenital disorders.

Schwartz-Jampel syndrome - myotonic chondrodystrophySynonym(s): Schwartz-Jampel-Aberfeld syndrome

Schwartz-Jampel-Aberfeld syndrome - Synonym(s): Schwartz-Jampel syndrome

Medical Eponyms © Farlex 2012