Results 31 to 40 of about 1,086 (157)

Posterior Olecranon Fracture Dislocations in Adults: A Systematic Review

Orthopaedic Surgery, Volume 15, Issue 9, Page 2235-2243, September 2023., 2023
The posterior olecranon fracture‐dislocations should be considered independently and separately with other types of posterior Monteggia lesions. The main characteristics of posterior olecranon fracture dislocations (POFDs) are disruptions of trochlear notch including the olecranon and coronoid processes and severe radial head fractures, while the ...
Jie Xiong, Jiyong Yang, Lian Luo, Maoqi Gong   +3 more
wiley   +1 more source

Clinical heterogeneity of NADSYN1‐associated VCRL syndrome

Clinical Genetics, Volume 104, Issue 1, Page 114-120, July 2023., 2023
Clinicians should suspect NAD deficiency disorder when a patient presents with congenital malformations, especially when vertebral, cardiac, renal, or limb defects are present. We expanded NAD deficiency disorder spectrum with the presentation of three cases from two unrelated families, with high inter‐ and intra‐familial variability.
Marion Aubert‐Mucca, Caroline Janel, Valérie Porquet‐Bordes, Olivier Patat, Renaud Touraine, Thomas Edouard, Caroline Michot, Aude Tessier, Valérie Cormier‐Daire, Tania Attie‐Bitach, Geneviève Baujat   +10 more
wiley   +1 more source

Surgical Treatment of Congenital Radioulnar Synostosis in Children: Systematic Review [PDF]

Travmatologiâ i Ortopediâ Rossii, 2022
Background. Congenital radioulnar synostosis (CRUS) may have a negative impact on the function of the upper limb and cause disability. The main aim of the surgical treatment is to correct the forearm position for diminishing functional limitations ...
Yulia A. Fedorova, Sergei V. Vissarionov, Yaroslav N. Proschenko, Sofia A. Gevorgiz, Ekaterina A. Zakharyan   +4 more
doaj   +1 more source

Congenital proximal radioulnar synostosis

Indian Journal of Plastic Surgery, 2003
Congenital proximal radio-ulnar synostosis is a rare anomaly and is often part of syndromes such as Crouzon, Apert's and Poland's. We have successfully managed one such case with bilateral involvement not associated with any other congenital deformity ...
B. B. Dogra, Manmohan Singh, Anil Malik
doaj   +3 more sources

MECOM-associated syndrome: a heterogeneous inherited bone marrow failure syndrome with amegakaryocytic thrombocytopenia

Blood Advances, 2018
: Heterozygous mutations in MECOM (MDS1 and EVI1 complex locus) have been reported to be causative of a rare association of congenital amegakaryocytic thrombocytopenia and radioulnar synostosis.
Manuela Germeshausen, Phil Ancliff, Jaime Estrada, Markus Metzler, Eva Ponstingl, Horst Rütschle, Dirk Schwabe, Richard H. Scott, Sule Unal, Angela Wawer, Bernward Zeller, Matthias Ballmaier   +11 more
doaj   +1 more source

Familial radioulnar synostosis. [PDF]

Journal of Medical Genetics, 1978
A family with proximal radioulnar synostosis segregating in three generations is described. Familial radioulnar synostosis is a rare anomaly; however, the sporadic form is a frequent feature in cases of sex chromosome abnormalities and other syndromes.
openaire   +2 more sources

Congenital radioulnar synostosis: A report of 11 cases and review of literature [PDF]

Acta Medica Iranica, 2002
During the last 10 years, we have had 11 cases of radioulnar (RU) synostosis, a very rare congenital amomaly of the upper extremity. Only 3 of them required surgical intervention.
Farzan M, Daneshjou Kh, Mortazavi SMJ, Espander R   +3 more
doaj   +2 more sources

Congenital bilateral radioulnar synostosis with acute lymphoblastic leukemia: A case report

Journal of Applied Hematology, 2017
Radioulnar synostosis (RUS) is a rare, congenital bone anomaly characterized by fusion of the radius and the ulna. RUS occurs more often in males than in females and is bilateral in 50% of the cases.
Rahaf M Qari, S K Aljaouni
doaj   +1 more source

Warfare, Labor, and Urban Stress: Divergent Health Trajectories in Mongol‐Period Karakorum

International Journal of Osteoarchaeology, Volume 36, Issue 4, Page 954-969, July/August 2026.
ABSTRACT This study examines major palaeopathological trends in Mongol‐period Karakorum and incorporates them into the existing body of research in order to deepen our understanding of health and survival, the impacts of conflict and violence on past populations, and the lived experiences of the city's diverse inhabitants within the broader socio ...
Júlia Olive‐Busom, Susanne Reichert, Dunburee Batsukh, Jan Bemmann, Alice Toso   +4 more
wiley   +1 more source

SMAD6-deficiency in human genetic disorders

npj Genomic Medicine, 2022
SMAD6 encodes an intracellular inhibitor of the bone morphogenetic protein (BMP) signalling pathway. Until now, SMAD6-deficiency has been associated with three distinctive human congenital conditions, i.e., congenital heart diseases, including left ...
Ilse Luyckx, Aline Verstraeten, Marie-José Goumans, Bart Loeys   +3 more
doaj   +1 more source