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Singleton Merten syndrome

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Medical condition

Singleton Merten syndrome
Other names	Singleton-Merten dysplasia
Singleton Merten syndrome is inherited in an autosomal dominant manner.

Singleton Merten syndrome is an autosomal dominant genetic disorder with variable expression with an onset of symptoms during childhood.

Signs and symptoms[edit]

The patients often present with a historyoffever of unknown origin, muscular weakness, poor development, abnormal dentition, normal serum calcium, phosphorus, and alkaline phosphatase levels. Associated clinical findings also include glaucoma, photosensitivity, heart block, foot deformities, and chronic psoriasiform skin lesions.^{[citation needed]}

Genetics[edit]

This condition has been associated with mutations in the retinoic acid-inducible gene I (DDX58) and melanoma differentiation-associated protein 5 (IFIH1) genes.^[1]

Diagnosis[edit]

Radiological findings[edit]

The classic radiologic findings were first described by Edward B. Singleton and David Merten in 1973.^{[citation needed]}

Typical radiographic appearances include skeletal demineralization, expanded shafts of the metacarpals and phalanges with widened medullary cavities, cardiomegaly, and intramural calcification of the proximal aorta with occasional extension into the aorticormitral valves.^{[citation needed]}

Other commonly seen radiographic findings include shallow acetabular fossa, subluxation of the femoral head, coxa valga, hypoplastic radial epiphysis, soft tissue calcifications between the radius and ulna, constriction of the proximal radial shaft, acro-osteolysis, and equinovarus foot deformities.^{[citation needed]}

Treatment[edit]

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Sources[edit]

• Singleton, EB, Merten DF: An unusual syndrome of widened medullary cavities of the metacarpals and phalanges, aortic calcification and abnormal dentition, Pediatric Radiol 1:2, 1973.
• [1] Resources form the National Institutes of Health
• [2] WebMD information

References[edit]