Results 21 to 30 of about 962,864 (203)

Hereditary neuropathy with liability to pressure palsy – epidemiology and diagnosis

Aktualności Neurologiczne, 2018
The aim of the work is to present current knowledge on epidemiology, causes, symptomatology and diagnosis of hereditary neuropathy with liability to pressure palsy.
Dominik Siutka, Katarzyna Bonek, Małgorzata Fudala, Waldemar Brola   +3 more
doaj   +1 more source

Peripheral nerve entrapments—rare causes of a common condition: case series

Autopsy and Case Reports, 2021
Compressive syndromes of peripheral nerves both in the upper and lower limbs are part of daily clinical practice; however, the etiological diagnosis can be challenging and impact on the outcome of the patient. We report five cases with rare etiologies of
Laura Mendes de Barros, Adilson Jose Manuel de Oliveira, Alan de Souza Santos, Flávio Leão Lima, Rodolfo Silva Valente   +4 more
doaj  

An Accessory Abductor Digiti Minimi as Possible Risk Factor of the Median and Ulnar Nerves Compression

, 2020
During routine dissection of a left upper limb of a 68-year-old male human cadaver, an unusual muscle was observed originating from the radius and flexor retinaculum, and continued in the hypothenar region with the muscle belly of the abductor digiti ...
López Fernández, Pedro, Morán Morán, Julio, Murillo González, Jorge Alfonso, Catón Vázquez, Francisco Javier, Martínez Sanz, Elena   +4 more
core   +1 more source

Outcomes after Anterior Interosseous Nerve to Ulnar Motor Nerve Transfer

, 2023
Background  Ulnar nerve lesions proximal to the elbow can result in loss of intrinsic muscle function of the hand. The anterior interosseous nerve (AIN) to deep motor branch of the ulnar nerve (DBUN) transfer has been demonstrated to provide intrinsic ...
Gross, Jeffrey N., Borschel, Gregory H., Dawson, Steven E., Loewenstein, Scott, Adkinson, Joshua M., Wu, Gerald J.   +5 more
core   +1 more source

Síndrome do canal de Guyon causada por cisto sinovial Guyon's canal syndrome due to a synovial cyst

Revista Brasileira de Ortopedia, 2010
Apresentamos um caso de síndrome do canal de Guyon por um cisto sinovial no punho esquerdo de uma paciente do sexo feminino, de 48 anos. A paciente apresentava dor e parestesia na topografia do nervo ulnar, diminuição da força muscular e deformidade na ...
Evandro Silva Ruas, Rodrigo Simões Castilho, Philipe Eduardo Carvalho Maia, Gustavus Lemos Ribeiro Melo   +3 more
doaj   +1 more source

Ulnar nerve entrapment syndromes and their therapy

, 2021
Nervus ulnaris je po nervus medianus druhým nejčastěji postiženým periferním nervem kompresní neuropatií. Ke kompresi nervu dochází nejčastěji v kubitálním tunelu.
Kuneš, Lukáš
core  

A Rare Form of Microcephalic Primordial Dwarfism due to NSMCE2 Deficiency (Seckel Syndrome Type 10): A Report of Macular Involvement

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Biallelic variants in NSMCE2 (MMS21), which encodes the SUMO E3 ligase subunit of the SMC5/6 chromatin‐maintenance complex, have recently been implicated in microcephalic primordial dwarfism (MPD), corresponding to Seckel syndrome type 10 (OMIM #617246).
Cristina Peduto, Céline Huber, Clément Paya, Isabelle Audo, Nathalie Boddaert, Valérie Cormier‐Daire   +5 more
wiley   +1 more source

Resultados da descompressão e anteriorização do nervo ulnar no cotovelo Results of ulnar nerve descompression and anterior transposition at the elbow

Revista Brasileira de Cirurgia Plástica, 2011
INTRODUÇÃO: A compressão do nervo ulnar no cotovelo é a segunda causa mais frequente de neuropatia compressiva no membro superior. Na maioria dos casos, a compressão ocorre no canal cubital, vulnerável à compressão extrínseca, intrínseca ou idiopática. O
Kátia Torres Batista, Hugo José de Araújo, Aloysio Campos da Paz Júnior   +2 more
doaj   +1 more source

Spectrum of Congenital Anomalies in Myhre Syndrome—Insights Into Effects Brought by Altered TGF‐β Signaling via Gain‐of‐Function Variants in SMAD4

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is a rare genetic disorder characterized by progressive multisystem involvement. Gain‐of‐function missense heterozygous variants affecting the Ile500 residue and Arg496 residue of the SMAD4 gene are implicated in this condition.
Kawmadi Gunawardena, Alessandro De Falco, Deborah Osio, Eleanor Sherlock, Emma Kivuva, Erina Sasaki, Francis H. Sansbury, Nayana Lahiri, Patricia Foley, Sahar Mansour, Shane McKee, Tazeen Ashraf, Nicola Brunetti‐Pierri, Usha Kini   +13 more
wiley   +1 more source

Acute Cubital Tunnel Syndrome Secondary to Anconeus Epitrochlearis Muscle

Journal of Orthopaedics, Trauma and Rehabilitation, 2015
Cubital tunnel syndrome is the most common type of ulnar nerve entrapment that usually associates with chronic sensory and motor symptoms. Having anconeus epitrochlearis muscle is an uncommon cause of cubital tunnel syndrome.
Ying-Kan Law
doaj   +1 more source