Zobrazeno 1 - 10
of 815
pro vyhledávání: '"congenital abnormality"'
Publikováno v:
Radiology Case Reports, Vol 20, Iss 1, Pp 23-26 (2025)
Hypoplasia of the internal carotid artery is a rare congenital abnormality that can present with an ischemic stroke or transient ischemic attacks. We present the case of a 17-year-old male who presented with right hemiparesis and dysarthria. The imag
Externí odkaz:
https://doaj.org/article/7f20f2a2b9b54312b57a1abd61dc744a
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 18, Iss 10, Pp 03-05 (2024)
Arnold Chiari Malformation (ACM) is a group of deformities of the cranium and hindbrain, where there is herniation of cerebellar tonsils through the foramen magnum. Based on the morphology and degree of anatomic defects, Chiari malformations are cate
Externí odkaz:
https://doaj.org/article/88a82ef11eab4b378e83fb14f3ca69ad
Autor:
Atiene S. Sagay, Szu-Chia Hsieh, Yu-Ching Dai, Charlotte Ajeong Chang, Jerry Ogwuche, Olukemi O. Ige, Makshwar L. Kahansim, Beth Chaplin, Godwin Imade, Michael Elujoba, Michael Paul, Donald J. Hamel, Hideki Furuya, Ricardo Khouri, Viviane Sampaio Boaventura, Laíse de Moraes, Phyllis J. Kanki, Wei-Kung Wang
Publikováno v:
International Journal of Infectious Diseases, Vol 139, Iss , Pp 92-100 (2024)
Objectives: Chikungunya virus (CHIKV), a reemerging global public health concern, which causes acute febrile illness, rash, and arthralgia and may affect both mothers and infants during pregnancy. Mother-to-child transmission (MTCT) of CHIKV in Afric
Externí odkaz:
https://doaj.org/article/c4029133a24a4961917f96d325203506
Publikováno v:
Journal of Clinical Interventional Radiology ISVIR, Vol 08, Iss 01, Pp 065-067 (2024)
The knowledge of different anatomic venous variants of central vessels is essential to improve the safety of procedures like central venous access and tunneled central catheter (TCC) placement. Persistent left superior vena cava (PLSVC) is an uncommo
Externí odkaz:
https://doaj.org/article/7a9664777bf749dd9001d3c807dfae21
Publikováno v:
Xin yixue, Vol 54, Iss 12, Pp 849-854 (2023)
Protein O-mannosyl-transferase 1 (POMT1) gene-encoded protein participates in the initial step of protein O-mannosylation modification and plays an important role in various physiological processes,such as cell connection and neuronal migration
Externí odkaz:
https://doaj.org/article/7733f223b65a430db3e39d890379a0e0
Publikováno v:
Radiology Case Reports, Vol 18, Iss 9, Pp 3236-3239 (2023)
Pulmonary sequestration is a rare congenital bronchopulmonary malformation with an estimated incidence of less than 6%. It is described as the abnormal formation of nonfunctional lung tissue that receives its blood supply from systemic circulation ra
Externí odkaz:
https://doaj.org/article/439d19c85eef4479a4ccee3a25facfcb
Publikováno v:
Veterinary Medicine and Science, Vol 9, Iss 2, Pp 712-716 (2023)
Abstract Aortic valve malformation is a common congenital abnormality reported in human medicine. The malformation is characterised by an increased or decreased number of cusps. Anatomical variations of the aortic valve that have been documented in h
Externí odkaz:
https://doaj.org/article/89fe64525a704ce9bc051959fa85380d
Autor:
Fatima Zahra Laabouri, Chelsea Folmar, Vicente Avila Reyes, Erin Beasley, Clare Ryan, Corrie Brown
Publikováno v:
Frontiers in Veterinary Science, Vol 10 (2023)
Abomasal ulcers, an economic concern for all calf-raising farms, are usually silent until perforation occurs, at which time management is complicated and often unrewarding. This case study describes perforating ulcer in a 3-day-old Brahman heifer, oc
Externí odkaz:
https://doaj.org/article/7dcca5a418ac473681be4a45e690d4ae
Autor:
Sepideh Shakeri, Narjes Soltani, Mohammad Reza Javan, mehrnaz abdolalian, Hossein Ayatollahi, fatemeh shams
Publikováno v:
Medical Laboratory Journal, Vol 17, Iss 1, Pp 42-46 (2023)
Background and objectives: Fanconi anemia (FA) is an autosomal recessive disorder that usually manifest in forms of pancytopenia, hyperpigmentation, and skeletal complications. Mutation in the DNA repair regulatory genes is associated with the develo
Externí odkaz:
https://doaj.org/article/89faa1ca7db941e2a2c4a21eea98193e
Publikováno v:
American Journal of Perinatology Reports, Vol 13, Iss 03, Pp e40-e43 (2023)
Unilateral lung agenesis is a rare congenital abnormality that typically presents with respiratory distress after birth. Prognostic factors include the side of the lung affected along with the presence or absence of other congenital abnormalities. Pr
Externí odkaz:
https://doaj.org/article/dec9a13ecf1649ae9b997142752872e7