Results 11 to 20 of about 117,358 (311)
Althea Medical Journal, 2017 Background: Congenital anomaly is a disease of structural or functional alteration since birth. The cause of congenital anomaly is genetic, environtment, and unknown.
Pradistya Syifa Yudiasari +2 more
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Scrotoschisis: A rare congenital urologic anomaly
Journal of Pediatric Surgery Case Reports, 2018 Background: Scrotoschisis is a rare congenital anomaly of the scrotal wall with idiopathic etiology it represents as congenital extrusion of the testis through the scrotal wall and its pathology is extremely rare.
Mohamed Mahfouz
doaj +2 more sources
Human Vaccines & Immunotherapeutics, 2018 Limited safety data are available on inadvertent exposure to quadrivalent human papillomavirus vaccine (4vHPV) during pregnancy. We conducted a descriptive observational postlicensure safety surveillance study in Kaiser Permanente Southern California and
Lina S. Sy +12 more
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International Journal of General MedicineBiniam Endale Geleta, Girma Seyoum Department of Anatomy, Addis Ababa University, Addis Ababa, EthiopiaCorrespondence: Biniam Endale Geleta, Email benjaminbig12@gmail.comBackground: Children with DS are at higher risk of developing congenital anomalies ...
Geleta BE, Seyoum G
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Sirenomelia- A rare congenital anomaly: Case report. [PDF]
J Educ Health Promot, 2023 Sirenomelia is an extremely uncommon congenital deformity in which neonate has fused lower limbs associated with various visceral malformations including urogenital and gastrointestinal tract, pulmonary hypoplasia, and potter's facies.
Thombare D, Dixit P, Chavan A, Najan A.
europepmc +2 more sources
Frontiers in Pediatrics, 2021 Background: Hypoplastic Left Heart Syndrome (HLHS) is a severe congenital heart defect (CHD) characterised by the underdevelopment of the left side of the heart with varying levels of hypoplasia of the left atrium, mitral valve, left ventricle, aortic ...
Kate E. Best +6 more
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Behçet’s disease in Wales: an epidemiological description of national surveillance data
Orphanet Journal of Rare Diseases, 2022 Objectives Behçet’s disease is a rare, chronic, incurable, multisystemic disease. It causes significant morbidity, with patients experiencing symptoms including mucous membrane ulcers, and joint pain and swelling.
Annie Ashman +3 more
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Congenital absence of superior vena cava – case report and review of the literature [PDF]
Romanian Journal of Pediatrics, 2020 Superior vena cava (SVC) agenesis or total congenital absence of superior vena cava is a very rare vascular anomaly, mainly asymptomatic throughout neonatal period.
Andreea Vidru +7 more
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The first 3D analysis of the sphenoid morphogenesis during the human embryonic period
Scientific Reports, 2022 The sphenoid has a complicated shape, and its morphogenesis during early development remains unknown. We aimed to elucidate the detailed morphogenesis of the sphenoid and to visualize it three-dimensionally using histological section (HS) and phase ...
Natsuko Utsunomiya +5 more
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Congenital fusion of cervical vertebrae: a review on embryological etiology [PDF]
Reviews in Clinical Medicine, 2016 Congenital fusion of cervical vertebrae is a rare anomaly. In this condition, two fused vertebrae appear structurally and functionally as one. This anomaly may be symptomatic or asymptomatic.
Mohammad Mardani +2 more
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