Results 21 to 30 of about 17,945 (251)
Further characterization of NFIB‐associated phenotypes: Report of two new individuals
American Journal of Medical Genetics Part A, Volume 191, Issue 2, Page 540-545, February 2023., 2023 Abstract Nuclear Factor I B (NFIB) haploinsufficiency has recently been identified as a cause of intellectual disability (ID) and macrocephaly. Here we report on two new individuals carrying a microdeletion in the chromosomal region 9p23‐p22.3 containing NFIB.
Gemma Marinella +8 more
wiley +1 more source
PLoS Neglected Tropical Diseases, 2021 Background Ethiopia aims to eliminate lymphatic filariasis by 2020, through a dual approach of mass drug administration to interrupt transmission and morbidity control which includes making hydrocele surgery available in all endemic areas.
A. Beyene +12 more
semanticscholar +1 more source
American Journal of Medical Genetics Part A, Volume 191, Issue 2, Page 332-337, February 2023., 2023 Abstract GTF2IRD1, a gene on chromosome 7 which encodes a transcription factor, is of significant clinical interest due to its heterozygous loss as part of the classical deletion associated with Williams–Beuren syndrome (WBS). However, biallelic variants in GTF2IRD1 alone as part of an autosomal recessive disease have not been previously reported. Here,
Christopher Thomas Cummings +1 more
wiley +1 more source
A mechanism for chronic filarial hydrocele with implications for its surgical repair. [PDF]
PLoS Neglected Tropical Diseases, 2010 BACKGROUND: Chronic hydrocele is the most common manifestation of bancroftian filariasis, an endemic disease in 80 countries. In a prospective study, we evaluated the occurrence of intrascrotal lymphangiectasia, gross appearance/consistency of the testis,
Joaquim Norões, Gerusa Dreyer
doaj +1 more source
PLoS ONE, 2021 BackgroundHydrocele is a chronic condition in males in which there is an excessive collection of straw-colored fluid, which leads to enlargement of the scrotum.
Choden Lama Yonzon +5 more
doaj +1 more source
Multifactorial Etiology of Sertoli Cell-Only Syndrome: A Rare Case Report. [PDF]
Clin Case RepABSTRACT This rare case from Pakistan highlights the multifactorial etiology of Sertoli Cell Only Syndrome, emphasizing the importance of early identification and management of contributing factors such as trauma, varicocele, and surgical interventions to improve fertility outcomes.
Gohar A +5 more
europepmc +2 more sources
Hydrocele in Pediatric Population.
Acta medica, 2020 Hydrocele is a collection of fluid within the tunica vaginalis. Based upon the etiology and the pathophysiology, it is divided into, the primary and secondary.
I. Patoulias +5 more
semanticscholar +1 more source
Unlocking Trust in Community Health Systems: Lessons From the Lymphatic Filariasis Morbidity Management and Disability Prevention Pilot Project in Luangwa District, Zambia [PDF]
International Journal of Health Policy and Management, 2022 Background Surgery for hydrocele is commonly promoted as part of morbidity management and disability prevention (MMDP) services for lymphatic filariasis (LF).
Joseph M. Zulu +8 more
doaj +1 more source
Indian Journal of Anaesthesia, 2020 Background and Aims: Hypotension is one of the most common side effects of spinal anaesthesia and preoperative volume status is one of the predictive variables for developing spinal-induced hypotension (SIH).
Basavaraja Ayyanagouda +5 more
semanticscholar +1 more source
Bilateral Hydrocele of the Canal of Nuck: A Rare Presentation in an Adult Female
International Medical Case Reports Journal, 2020 Hydrocele of the canal of Nuck is one of the rarest clinical entities in the female population. It occurs due to the failure of obliteration of the processus vaginalis, which is the extension of the parietal peritoneum.
S. Baral +3 more
semanticscholar +1 more source