Results 41 to 50 of about 2,909 (206)

Schmallenberg virus pathogenesis, tropism and interaction with the innate immune system of the host [PDF]

, 2013
Schmallenberg virus (SBV) is an emerging orthobunyavirus of ruminants associated with outbreaks of congenital malformations in aborted and stillborn animals.
A Bridgen, A Bridgen, A Kohl, AC Lowen, AJ Della-Porta, Alain Kohl, Andrew Shaw, Anna Janowicz, AR Elbers, B Hoffmann, B Xu, CA Evans, Catherine Lamm, Claudio Murgia, CM Southam, CT Walter, D Thomas, DH Cybinski, Esther Schnettler, Eva McGregor, F Arnaud, Friedemann Weber, G Barry, G Blakqori, G Blakqori, G Neumann, Gerald Barry, Ilaria M. Piras, JI Gillespie, JL Farmer, K Kupferschmidt, K Peperkamp, K Terasaki, K Wernike, KE Jones, Kerstin Hahn, KV Goller, LD Rasmussen, M Beer, M Bouloy, M Caporale, M Dominguez, M Palmarini, M Ratinier, M Spiegel, M Varela, Mandy Glass, Marco Caporale, Mariana Varela, Martin Beer, Massimo Palmarini, Melanie McFarlane, MJ Killip, MM Garigliany, MM Garigliany, NR Saunders, OR Causey, P Vialat, PJ Hotez, PT Leisnham, R Muller, RS Azevedo, S Shimshony, SE Randolph, T Ikegami, T Yanase, UJ Buchholz, V Herder, Vanessa Herder, VH Leonard, Wolfgang Baumgärtner, X Shi, Y Ogawa, YK Liao   +73 more
core   +3 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

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

Distal arthrogryposis with variable clinical expression caused by TNNI2 mutation [PDF]

, 2016
Distal arthrogryposis (DA) is a clinically and genetically heterogeneous disorder with multiple joint contractures. We describe a female DA patient with hand and foot deformities, and right-sided torticollis. Using exome sequencing, we identified a novel
Janković, Sunčana, Matsumoto, Naomichi, Miyake, Noriko, Ogata, Kazuhiro, Petrović, Davor, Shiina, Masaaki, Čulić, Vida, Đapić, Tomislav, Šimunović, Marko   +8 more
core   +1 more source

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

Surgical correction of a double congenital hernia in a veal calf

Veterinary Record Case Reports, Volume 14, Issue 2, May 2026.
Abstract This clinical case report describes the rare occurrence and successful surgical management of two simultaneous congenital hernias, umbilical and perineal, in a crossbred veal calf. At 5 days of age, the animal, weighing approximately 40 kg, showed visible swelling in the umbilical and perineal regions together with a congenital tail ...
Andrea Spadaro, Veronica Cristina Neve, Giovanna Lucrezia Costa, Roberto Puleio, Filippo Spadola   +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

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