Results 21 to 30 of about 1,080 (150)

Imperforate Hymen: A Comprehensive Systematic Review [PDF]

open access: yesJournal of Clinical Medicine, 2019
Keum Hwa Lee, Jae I L Shin
exaly   +2 more sources

Familial imperforate hymen among three sisters of varying ages from the same mother: Case report about an unusual family event

open access: yesJournal of Pediatric Surgery Case Reports, 2023
Imperforate hymen is a rare condition, occurring in 1 in 2000 females in childhood period. However, it is not an uncommon cause of lower abdominal pain in girls.
Jeannot M. Baanitse   +4 more
doaj   +1 more source

Knowledge of child abuse and neglect in nursing students: Assessment and perspectives

open access: yesJournal of Forensic Sciences, Volume 68, Issue 6, Page 2012-2020, November 2023., 2023
Abstract Misdiagnosis of child abuse and neglect can delay early treatment. Some authors have pointed out that nurses can miss child abuse and neglect diagnoses due to a lack of knowledge. It is unclear whether the lack of knowledge is due to students' insufficient preparation in nursing school and/or a deficiency in continuing education.
Francesco Lupariello   +2 more
wiley   +1 more source

Imperforate Hymen

open access: yesDonald School Journal of Ultrasound in Obstetrics and Gynecology, 2016
ABSTRACT An 11-year-old girl presented with pelvic pain for 2 weeks. Transabdominal ultrasound demonstrated a distended vagina filled with echogenic material consistent with blood. The uterus was visualized and was similarly distended. A diagnosis of hematocolpos and hematometria secondary to imperforate hymen was made.
Julie Hakim, Jennifer E. Dietrich
openaire   +2 more sources

Exome sequencing in a Romanian Bardet‐Biedl syndrome cohort revealed an overabundance of causal BBS12 variants

open access: yesAmerican Journal of Medical Genetics Part A, Volume 191, Issue 9, Page 2376-2391, September 2023., 2023
Abstract Bardet‐Biedl syndrome (BBS), is an emblematic ciliopathy hallmarked by pleiotropy, phenotype variability, and extensive genetic heterogeneity. BBS is a rare (~1/140,000 to ~1/160,000 in Europe) autosomal recessive pediatric disorder characterized by retinal degeneration, truncal obesity, polydactyly, cognitive impairment, renal dysfunction ...
Sheraz Khan   +17 more
wiley   +1 more source

Megalourethra and bladder foreign body in a female patient

open access: yesClinical Case Reports, Volume 11, Issue 6, June 2023., 2023
Foreign body in a female patient iatrogenically inserted via megalourethra. Key Clinical Message Undiagnosed female megalourethra can be a cause of iatrogenic bladder foreign body. Abstract Foreign bodies in the urinary bladder are relatively rare. Female megalourethra is an extremely rare congenital disorder which is usually associated with Müllerian ...
Vladimir Bilim   +3 more
wiley   +1 more source

Cervical Dysgenesis with Transverse Vaginal Septum with Imperforate Hymen in an 11 year old Girl Presenting with Acute Abdomen

open access: yesJournal of Nepal Medical Association, 2013
This case highlights the importance of careful evaluation of girls presenting with imperforate hymen as this is accompanied by other female reproductive tract anomalies. It is of utmost importance that a correct timely diagnosis is made so that the right
Pratiksha Gupta   +5 more
doaj   +3 more sources

CryptoImperforate Hymen with a Huge Abdominal Mass and Massive Hematocolpometra in a 15-Year-Old Girlmenorrhea with a Huge Abdominal Mass and Massive Hematocolpometra in a 15-Year-Old Girl

open access: yesBabcock University Medical Journal, 2023
Background: Imperforate hymen is one of the commonest embryological defects of the lower genital tract which occurs due to failure of canalization of the sinovaginal bulb. Its incidence is 1 in 2000 girls.
Oluwadare Martins Ipinnimo   +5 more
doaj   +1 more source

MNX1 mutations causing neonatal diabetes: Review of the literature and report of a case with extra‐pancreatic congenital defects presenting in severe diabetic ketoacidosis

open access: yesJournal of Diabetes Investigation, Volume 14, Issue 4, Page 516-521, April 2023., 2023
Abstract The MNX1 gene encodes a homeobox transcription factor found to be important for pancreatic beta cell differentiation and development. Mutations of the MNX1 gene that cause permanent neonatal diabetes mellitus (PNDM) are rare and have been reported in only two cases.
Hanan Hassan Aly   +3 more
wiley   +1 more source

Hematocolpos due to lower vaginal agenesis in an adolescent girl

open access: yesAcute Medicine &Surgery, Volume 10, Issue 1, January/December 2023., 2023
Hematocolpos due to vaginal agenesis with a functional uterus are particularly rare and are sometimes misdiagnosed in adolescent females because of the diversity in symptoms. Major complaints in cases diagnosed during adolescence are often lower abdominal pain, back pain, cancelation dysfunction, and primary amenorrhea.
Kazunori Imai   +8 more
wiley   +1 more source

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