Results 41 to 50 of about 2,876 (205)

Epidemiology and Emergence of Schmallenberg Virus Part 2: Pathogenesis and Risk of Viral Spread [PDF]

, 2016
Schmallenberg virus (SBV) is a novel Orthobunyavirus causing mild clinical signs in cows and malformations in aborted and neonatal ruminants in Europe. SBV belongs to the family Bunyaviridae and is transmitted by biting midges.
Coelho, Ana Cláudia, Cruz, Rita, Esteves, Fernando, Mesquita, João Rodrigo, Monteiro, António, Nóbrega, Cármen, Santos, Carla, Vala, Helena   +7 more
core   +2 more sources

Transverse cervical megapophysis as an uncommon cause of torticollis

Journal of Pediatric Surgery Case Reports, 2018
Congenital abnormalities of the spine are not uncommon in the general population and can be asymptomatic. Transverse megapophysis is a congenital anomaly manifested as an enlargement of the transverse processes, typically common in the lumbar vertebrae ...
Vito Pavone, Gianluca Testa, Ludovico Lucenti, Raffaele Falsaperla, Giuseppe Sessa   +4 more
doaj   +1 more source

Congenital muscular torticollis - a proposal for treatment and physiotherapy [PDF]

Rehabilitacja Medyczna, 2019
Congenital muscular torticollis (CMT) is a condition manifested by unilateral thickening and/or shortening of the sternocleidomastoid muscle. It can lead to local or global consequences (i.e., forced position and limitation of mobility of the cervical ...
Agata Michalska, Zbigniew Śliwiński, Justyna Pogorzelska, Marek Grabski, Jolanta Dudek, Małgorzata Szmurło, Maciej Szczukocki   +6 more
doaj   +1 more source

PRRT2 gene variant in a child with dysmorphic features, congenital microcephaly, and severe epileptic seizures: genotype-phenotype correlation? [PDF]

, 2019
BACKGROUND: Mutations in Proline-rich Transmembrane Protein 2 (PRRT2) have been primarily associated with individuals presenting with infantile epilepsy, including benign familial infantile epilepsy, benign infantile epilepsy, and benign myoclonus of ...
Cho SY, Corsello G, Falsaperla R., Jin DK, Marino S, Marino SD, Pappalardo XG, Pavone P, Ruggieri M   +8 more
core   +1 more source

A Rare Case of Spontaneous Intrauterine Skull Fracture

Acta Médica Portuguesa, 2020
Skull fractures are rare in newborns and normally caused by maternal abdominal trauma or complicated deliveries. However, in rare cases, these fractures are found in neonates born after an uneventful pregnancy and delivery.
Mariana Dória, Catarina Viveiros, Lia Rodrigues e Rodrigues, Fátima Soares   +3 more
doaj   +1 more source

Cervical scoliosis: clinical and radiographic outcomes [PDF]

, 2015
Study Design Retrospective study. Objective Cervical scoliosis is a rare condition that can arise from various etiologies. Few reports on the surgical management of cervical scoliosis exist.
Bakhsh, Wajeeh R, Chuntarapas, Tapanut, Mesfin, Addisu, Riew, K. Daniel   +3 more
core   +2 more sources

Chest wall fibromatosis with congenital muscular torticollis: Two forms of deep fibromatosis in a child

Journal of Indian Association of Pediatric Surgeons, 2018
Desmoid tumors (fibromatosis) are intermediate grade, locally aggressive soft-tissue tumors. A rare case of chest wall fibromatosis in a girl with congenital muscular torticollis is being reported.
Sachit Anand, Anjan K Dhua, Veereshwar Bhatnagar, Devasenathipathy Kandasamy, Sudheer Arava   +4 more
doaj   +1 more source

Diprosopus dirrhinus (nasal duplication) in a female Holstein Friesian calf: Clinical findings, diagnostic imaging and surgical management

Veterinary Record Case Reports, Volume 14, Issue 2, May 2026.
Abstract An 11‐week‐old Holstein Friesian heifer calf presented with a congenital nasal abnormality characterised by an additional, turbinate‐like structure located dorsally on the nasal bridge. Clinical examination of the calf revealed normal respiratory function, with the accessory structure producing mucoid discharge from blind‐ended cavities ...
Raffaela Marian, Michael J. S. Duggan, Clodagh M. Kearney, Antonella Puggioni, Eoin G. Ryan   +4 more
wiley   +1 more source

Late presentation of congenital muscular torticollis in siblings

Journal of Pediatric Surgery Case Reports, 2017
Congenital muscular torticollis (CMT) is the third most common congenital musculoskeletal anomaly seen in children. It is a condition in which the affected sternocleidomastoid muscle becomes a fibrosed cord with associated shortening of the muscle.
Sam Aruputha John, MS, MCh (ped surgery, India), Ahamed Faiz ali, MS, MRCS, FAMS (PEDSURG), Rasha kassem, Ali H. Ashkanani, MB, BCH, B.A.O(R.C.S.I), Ola Abdelfattah Taher, MSC (ped surgery), Hassan Ahmed Adly, MS (PEDSURG)   +5 more
doaj   +1 more source

Torticollis in Connection with Spine Phenotype

Diagnostics, 2022
Purpose: Torticollis is not of uncommon occurrence in orthopaedic departments. Various theories and studies concerning the pathogenesis of the deformity have been suggested. We aimed to highlight and discuss the underlying cervical and spine malformation
Ali Al Kaissi, Nabil Nassib, Sami Bouchoucha, Mohammad Shboul, Franz Grill, Susanne Gerit Kircher, Polina Ochirova, Sergey Ryabykh   +7 more
doaj   +1 more source