Chordee Without Hypospadias: Report of 79 Chinese Prepubertal Patients
نویسندگان
چکیده
منابع مشابه
Our experience in chordee without hypospadias: results of 102 cases.
PURPOSE We present long-term surgical experience of 102 chordee without hypospadias cases. MATERIALS AND METHODS This retrospective study included 102 chordee without hypospadias cases who were surgically treated between 1999 and 2012. Range of patients' age was from 1 month to 31 years. Seventy-two patients were adult, and 30 were children. Mean duration of follow up was 49.3 months. The pat...
متن کاملPathoembryology of Hypospadias and Chordee
Submit Manuscript | http://medcraveonline.com Abbreviations: AMH: Anti-Mullerian Hormone; AR: Androgen Receptors; ATF3: Activating Transcription Factor 3; CPAs: Congenital Penile Anomalies; CWH: Chordee Without Hypospadias; EDCs: Endocrine Disrupting Chemicals; KFS: Klinefelter Syndrome; LUTS: Lower Urinary Tract Symptoms; MAGPI: Meatal Advancement and Glanuloplasty Incorporated; SMR: Split Med...
متن کاملThe treatment of ventral penile chordee without hypospadias by dorsal midline plication in an adolescent boy
Herein we report of a case with isolated ventral penile chordee who underwent dorsal midline plication procedure. We aimed to present our experience and to review of the literature on current management.
متن کاملPrefabricated partial distal urethral in 2-staged repair of proximal hypospadias with severe chordee.
PURPOSE To describe a new technique for staged hypospadias repair in which the urethral plate is divided and tubularized transverse island flap prefabricated partial distal urethral at the time of the first stage. MATERIALS AND METHODS Sixteen patients with proximal hypospadias associated with severe chordee were operated on using a new staged technique. At the time of the first stage, the ur...
متن کاملPrepubertal Diagnosis of Klinefelter Syndrome: A Rare Case Report
Klinefelter syndrome is characterised by advancing testicular function deterioration causing aspermatogenesis and androgen deficiency. Klinefelter patients characteristically have complete male sex differentiation, and genital anomalies are infrequently associated. Penoscrotal malformations at birth are very rare in this syndrome. Nonetheless, it is important to know the association, as one of...
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ژورنال
عنوان ژورنال: Journal of Andrology
سال: 2007
ISSN: 0196-3635
DOI: 10.2164/jandrol.106.002436