Results 61 to 70 of about 3,659 (225)

Modified shehata surgery vs. laparoscopic One-stage orchiopexy for intra-abdominal cryptorchidism: a comparative retrospective study

open access: yesFrontiers in Surgery
ObjectiveTo compare the therapeutic outcomes of a modified Shehata surgery with a condensed 4-week interstage interval vs. conventional laparoscopic one-stage orchiopexy for intra-abdominal cryptorchidism.MethodsWe retrospectively analyzed 70 children ...
Shiyu Xiong   +7 more
doaj   +1 more source

Two cases of testicular torsion diagnosed by the ultrasonic Doppler method [PDF]

open access: yes, 1986
Two cases of testicular torsion diagnosed with ultrasonic Doppler method are reported. Case 1. A 17-year-old male noticed pain and swelling of the right intrascrotal contents during sleeping and visited our clinic.
中尾, 昌宏   +5 more
core  

Artificial Intelligence Software Changes Rare Disease Testing Strategy in Real Time: An International Case Series Using Face2Gene

open access: yesAmerican Journal of Medical Genetics Part A, Volume 197, Issue 11, November 2025.
ABSTRACT Genetic disorders commonly share features such as developmental delays, cognitive impairment, and behavioral challenges, yet many conditions also present unique dysmorphic features that distinguish them. Performing a thorough medical and family history and a detailed physical exam with attention to dysmorphic features is often the first step ...
Natasha L. Rudy   +15 more
wiley   +1 more source

Highly Complete Follow‐Up Data Are Necessary to Ascertain the Actual Complication Rate in Orchidopexy for Undescended Testes

open access: yesInternational Journal of Urology, Volume 32, Issue 10, Page 1482-1487, October 2025.
ABSTRACT Objective This study aimed to assess orchidopexy outcomes in a tertiary pediatric urology center. Methods A retrospective review of orchidopexies at our institution initially showed a 20% follow‐up loss. To ensure more reliable outcomes, patients and parents were actively contacted and encouraged to attend follow‐up visits 6 months post ...
Mick Uijldert   +6 more
wiley   +1 more source

Абдомінальна форма крипторхізму (особливості лікування) [PDF]

open access: yes, 2012
Останнім часом все більшої актуальності набувають питання чоловічого безпліддя через складну демографічну ситуацію, що склалась в Україні.
Волошин, Ю. Л.   +6 more
core  

Sexual Function, Fertility and Quality of Life after Modern Treatment of Anorectal Malformations [PDF]

open access: yes, 2016
Purpose: Sexual dysfunction and impaired quality of life due to fecal incontinence are common after classic operations for anorectal malformations. We hypothesized that modern repairs may result in improved outcomes.
Kyrklund, Kristiina   +3 more
core   +1 more source

Management of cryptorchidism in children: guidelines [PDF]

open access: yes, 2008
QUESTION: To develop clinical guidelines for the management of cryptorchidism in pre-pubertal boys, from early diagnosis through therapy to long-term follow-up and prognosis.
Burnand, B.   +8 more
core  

Orchidopexy san ligation technique of orchidopexy

open access: yesAfrican Journal of Paediatric Surgery, 2011
Pediatric hernia surgery is the most common operation done by pediatric general surgeons and it is a core competency for general surgeons in the developing world. Herniotomy is performed for the surgical repair of hernia and along with orchiopexy for the
Jain Vishal   +4 more
doaj  

停留精巣における精巣上体付着異常の臨床的検討 [PDF]

open access: yes, 2002
Purpose: Among the epididymal abnormalities observed at a relatively high rate in patients with undescended testis, we focused on the state of adhesion between the testis and the epididymis and evaluated the clinical significance of this condition.
加瀬 浩史
core  

Aarskog Syndrome: Deep Phenotyping and Genomic Landscape of a New Cohort Including Adult Patients

open access: yesClinical Genetics, Volume 108, Issue 3, Page 334-346, September 2025.
This study presents the deep phenotyping data of 14 new Aarskog‐Scott syndrome patients with molecular confirmation. ABSTRACT Aarskog‐Scott syndrome (AAS, MIM#305400) is an X‐linked disorder characterized by recognizable facial features, short stature, and genitourinary and skeletal malformations.
Gozde Tutku Turgut   +7 more
wiley   +1 more source

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