Radio-ulnar synostosis, unilateral

MedGen UID:: 1842614
•Concept ID:: C5679984
•: Congenital Abnormality

Synonyms:	Radio-ulnar fusion, unilateral; radio-ulnar fusion, unilateral; radio-ulnar synostosis, unilateral
Modes of inheritance:	Unknown inheritance MedGen UID: 989040 •Concept ID: CN307042 • Finding Source: Orphanet Hereditary clinical entity whose mode of inheritance is unknown. See: This record Unknown inheritance (Orphanet)

Monarch Initiative:	MONDO:0017554
Orphanet:	ORPHA295217

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVRadio-ulnar synostosis, unilateral

Joint formation defects
- Radioulnar synostosis
  - Radio-ulnar synostosis, unilateral

Recent clinical studies

Etiology

Leydig cell tumor in a patient with 49,XXXXY karyotype: a review of literature.

Maqdasy S, Bogenmann L, Batisse-Lignier M, Roche B, Franck F, Desbiez F, Tauveron I
Reprod Biol Endocrinol 2015 Jul 10;13:72. doi: 10.1186/s12958-015-0071-7. PMID: 26160035 Free PMC Article

Osteotomy of the synostosis mass for the treatment of congenital radio-ulnar synostosis.

Khalil I, Vizkelety T
Arch Orthop Trauma Surg 1993;113(1):20-2. doi: 10.1007/BF00440589. PMID: 8117505

Congenital radio-ulnar synostosis: surgical treatment.

Green WT, Mital MA
J Bone Joint Surg Am 1979 Jul;61(5):738-43. PMID: 457717

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