Congenital radioulnar synostosis

Congenital radioulnar synostosis is a rare bone disorder that may be isolated or associated with other disorders and that is characterized by failure of segmentation of the radius and ulna during embryological development, causing limited rotational movements of the forearm, which may lead to difficulties with some activities of daily living.



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Narrow down the case reports



Total: 9 (papers)

   


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)		 PMID
(PMCID)
1
(60.5%)		 16681404
 Pierre Robin sequence with esophageal atresia and congenital radioulnar synostosis.
Ozkan KU, Coban YK, Uzel M, Ergun M, Oksuz H.
Cleft Palate Craniofac J. 2006;43(3):317-20.
Glossoptosis Micrognathia
Esophageal Atresia Homo sapiens Infant, Newborn Male Pierre Robin Syndrome Tracheoesophageal Fistula
2
(39.7%)		 9730128
 Mobilization of a congenital proximal radioulnar synostosis with use of a free vascularized fascio-fat graft.
Kanaya F, Ibaraki K.
J Bone Joint Surg Am. 1998;80(8):1186-92.
Radioulnar synostosis
Child Fascia Homo sapiens Male Osteotomy
3
(37.8%)		 23752153
 Treatment of blocked elbow flexion in congenital radioulnar synostosis with radial head excision: a case series.
VanHeest AE, Lin TE, Bohn D.
J Pediatr Orthop. 2013;33(5):540-3.
Dislocated radial head
Child Child, Preschool Females Follow-Up Studies Homo sapiens Male Pain Range of Motion, Articular Time Factors
3
(37.8%)		 2216544
 Imaging rounds #103. Myositis ossificans in association with congenital radioulnar synostosis and congenital anterior radial head dislocation.
Luke DL, Manske PR, Gilula LA.
Orthop Rev. 1990;19(8):714-6, 719-20.
Anterior radial head dislocation
Adult Homo sapiens Male Myositis Ossificans
5
(21.2%)		 18823611
 [Congenital radioulnar synostosis].
Al-Saadi ZS, Havekrog BH.
Ugeskr Laeger. 2008;170(40):3147-8.
Radial head subluxation
Child, Preschool Females Homo sapiens
6
(20.4%)		 17878844
 [Fracture of the two forearm bones and congenital radioulnar synostosis: a case report].
Mathieu L, Ollat D, Versier G.
Rev Chir Orthop Reparatrice Appar Mot. 2007;93(5):511-4.
Ankylosis
Follow-Up Studies Fracture Fixation, Internal Homo sapiens Male Nonpenetrating Wounds Pronation Radius Fractures Supination Time Factors Torsion, Mechanical Ulna Fractures
6
(20.4%)		 15880988
 Congenital radioulnar synostosis treated using a microvascular free fasio-fat flap.
Kao HK, Chen HC, Chen HT.
Chang Gung Med J. 2005;28(2):117-22.
Ankylosis
Child Fascia Females Homo sapiens Surgical Flaps
8
(4.0%)		 21385658
 De novo interstitial deletion of chromosome 2 (p23p24).
Su PH, Chen JY, Tsao TF, Chen SJ.
Pediatr Neonatol. 2011;52(1):46-50.
Hearing impairment
Child Chromosome Deletion Chromosomes, Human, Pair 2 Developmental Disabilities Homo sapiens Limb Deformities, Congenital Magnetic Resonance Imaging Male X-Ray Computed Tomography
8
(4.0%)		 18177653
 Congenital radioulnar synostosis, azoospermia, and pseudodicentric Y chromosome.
Syed AA, Quinton R.
Fertil Steril. 2008;90(2):425-6.
Azoospermia
Adult Azoospermia Chromosomes, Human, Y Homo sapiens Male Sex Chromosome Aberrations Sex Chromosome Disorders
        

Phenotype(s) retrieved from Orphanet

    Total: 0

HPO ID Term Frequency


Phenotype(s) retrieved from case reports

    Total: 6

HPO ID Term # of case reports
HP:0000027 Azoospermia 1
HP:0000162 Glossoptosis 1
HP:0000201 Pierre-Robin sequence 1
HP:0000347 Micrognathia 1
HP:0005084 Anterior radial head dislocation 1
HP:0100614 Myositis 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID