Results 21 to 30 of about 2,683 (132)

Prevalence of pectus excavatum (PE), pectus carinatum (PC), tracheal hypoplasia, thoracic spine deformities and lateral heart displacement in thoracic radiographs of screw-tailed brachycephalic dogs.

PLoS ONE, 2019
Pectus excavatum, thoracic spine deformities, tracheal hypoplasia and lateral heart displacement are frequently described in brachycephalic dog breeds. Pectus carinatum is described sporadically, although the authors' observations demonstrate that it may
Renata Komsta, Zbigniew Osiński, Piotr Dębiak, Piotr Twardowski, Barbara Lisiak   +4 more
doaj   +1 more source

Anesthesia for minimally invasive chest wall reconstructive surgeries: Our experience and review of literature

Saudi Journal of Anaesthesia, 2017
Minimal access procedures have revolutionized the field of surgery and opened newer challenges for the anesthesiologists. Pectus carinatum or pigeon chest is an uncommon chest wall deformity characterized by a protruding breast bone (sternum) and ribs ...
Shagun Bhatia Shah, Uma Hariharan, Ajay Kumar Bhargava, Laleng M Darlong   +3 more
doaj   +1 more source

Pectus Excavatum / Pectus Carinatum: tratamento cirúrgico

Revista do Colégio Brasileiro de Cirurgiões
OBJETIVO: Apresentar os resultados obtidos com técnica única para tratamento do Pectus Excavatum e Pectus Carinatum. MÉTODO: De 1976 a 2000 foram operados, 183 portadores de Deformidades da Parede Torácica Anterior sendo 98 Pectus Carinatum (70 P ...
Marlos de Souza Coelho, Wilson de Souza Stori Júnior, Lauro Del Valle Pizarro, Sérgio Augusto Zanin, José Lino Gonçalves, Nelson Bergonse Neto   +5 more
doaj   +1 more source

Pectus updates and special considerations in Marfan syndrome

Pediatric Reports, 2018
Congenital chest wall or pectus deformities including pectus excavatum (funnel chest) and pectus carinatum (pigeon chest) affect a significant proportion of the general population and up to 70% of patients with Marfan syndrome.
Stephanie Fraser, Anne Child, Ian Hunt
doaj   +1 more source

Síndrome de marfán con malformación ósea tipo pectus carinatum: reporte de un caso en Cartagena de indias. Colombia

Revista Ciencias Biomédicas, 2020
El síndrome de Marfán (MFS) es la enfermedad del tejido conectivo más común de origen  genético, con transmisión hereditaria autosómica dominante. La mutación se localiza en el gen  FBN1 que codifica para la proteína Fibrilina-1.
Dacia I. Malambo García, Gustavo J. Mora García, José C. Pomares Estrada, Cristian Gómez García (q.e.p.d.), Doris E. Gómez Camargo   +4 more
doaj   +1 more source

Pectus carinatum in a dog Pectus carinatum em um cão

Arquivo Brasileiro de Medicina Veterinária e Zootecnia, 2009
Descreve-se o atendimento de um cão macho de cinco meses de idade, apresentando diversas malformações congênitas, incluindo uma protrusão ventral da parte distal do externo, que foi diagnosticada como Pectus carinatum tendo por base os achados clínicos e
D.B. Souza, P.S.C. Andrade Júnior, C.M.A. Mariano, F.S. Costa, E.J. Abílio   +4 more
doaj   +1 more source

Pectus excavatum in osteogenesis imperfecta type I treated with Nuss procedure after pamidronate therapy

Journal of Pediatric Surgery Case Reports, 2021
Osteogenesis imperfecta is a genetic disorder caused by mutations in genes affecting type I collagen that is mostly found in bone, skin and tendons. In addition to bone fragility and increased risk of fractures, patients with osteogenesis imperfecta can ...
Nelimar Cruz Centeno, Victor N. Ortiz Justiniano   +1 more
doaj   +1 more source

Safe performance of spinal anesthesia in a critical patient with neurofibromatosis, pectus carinatum, and temporomandibular joint dysfunction: A case report

Patient Safety in Surgery, 2010
Background Neurofibromatosis is a syndrome caused by the abnormal deposition of neural tissues of the nervous system, endocrine system, visceral structures, and skin.
Zencirci Beyazit
doaj   +1 more source

Long‐term outcome after fetal endoscopic tracheal occlusion for congenital diaphragmatic hernia: systematic review

Ultrasound in Obstetrics &Gynecology, EarlyView.
Abstract Objective This systematic review aimed to evaluate the long‐term outcomes of infants who had undergone fetal endoscopic tracheal occlusion (FETO) for congenital diaphragmatic hernia (CDH). Methods PubMed, MEDLINE, EMBASE and the Cochrane Central Register of Controlled Trials (CENTRAL) were searched from inception to October 2025 for studies ...
S. Shah, R. Ruiz Roman, K. H. Nicolaides
wiley   +1 more source

Assessment of Growth in Cardio‐Facio‐Cutaneous Syndrome

American Journal of Medical Genetics Part A, Volume 200, Issue 11, Page 2443-2453, November 2026.
ABSTRACT Cardio‐facio‐cutaneous (CFC) syndrome is a rare, multiple congenital anomaly disorder in which individuals commonly experience faltering growth; however, systematic analysis of growth parameters in this disorder has not been performed. We recruited 69 participants with CFC through CFC International and collected data on assessing height ...
Kari Johnston, Sandesh C. S. Nagamani, Bradley S. Miller, Katherine A. Rauen, Richard D. Boyce, Salma Musaad, Pilar L. Magoulas   +6 more
wiley   +1 more source