[Smith-McCort syndrome (author's transl)].
Rofo, 1979/2;130(2):213-22.
PMID: 154455
Impact factor: 2.295
Abstract
An 13-year-old mentally normal boy with short-trunked dwarfism is discribed as a case of the Smith-McCort syndrome (SMC-syndrome). His disease has been observed radiologically, clinically an histologically for many years. According to Spranger (23) this disorder differs from the Dyggve-Melchior-Clausen disease (DMC-syndrome) by lacking oligophrenia. Beside a characteristic flattening of the vertebral bodies both syndromes show a lacelike appearance of the iliac crest (crest sign) as a significant radiological sign. Both syndromes appear to be inherited as an autosomal recessive trait.
MeSH terms
Adolescent; Diagnosis, Differential; Dwarfism; Foot; Hand; Humans; Hyaluronic Acid; Intellectual Disability; Male; Mucopolysaccharidoses; Radiography; Spine; Syndrome
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