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.

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.

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