نتایج جستجو برای: dysgenesis

تعداد نتایج: 2586  

Journal: :The Laryngoscope 2014
Michael E McCormick Brian K Reilly Jonathan G Murnick Joshua R Bedwell

OBJECTIVES/HYPOTHESIS We describe management of an infant with chronic aspiration as a result of severe and rarely described laryngeal dysgenesis. RESULTS A neonate with severe maldevelopment of the laryngeal structures required tracheostomy for respiratory distress on day-of-life 1, but the patient continued to have aspiration pneumonias. After failing to improve with conservative measures, ...

2016
Jyoti Taneja David Ogutu Michael Ah-Moye

Objective To report a rare successful pregnancy after fertility treatment in a patient with Swyer syndrome. Design Case report. Setting Herts & Essex Fertility Centre, Cheshunt, UK. Patients A 36-year-old patient with 46, XY gonadal dysgenesis. 31 year old husband with normal sperm analysis. Interventions Chromosomal analysis, Saline infusion sonography, Pipelle endometrial scratch, ICS...

Journal: :British Journal of Ophthalmology 1967

Journal: :Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 1991

2017
Masashi Kubota Naoki Terada Katsuhiro Ito Hideaki Takada Toshihiro Magaribuchi Atsuro Sawada Shusuke Akamatsu Hiromitsu Negoro Ryoichi Saito Takashi Kobayashi Toshinari Yamasaki Takahiro Inoue Osamu Ogawa

A case of a 45,X/46,XY boy with gonadal dysgenesis is presented. The patient showed hypospadias and right undescended testis. He underwent underwent repair surgery for hypospadias, right orchidopexy, and bilateral testicular biopsy. Testicular biopsy revealed no malignant finding. He was followed-up annually by scrotum palpation. When the patient grew up to 24 years old, he was diagnosed to hav...

2016
Sriharibabu Manne C. H. Veeraabhinav Mounica Jetti Yalamanchali Himabindu Kiranmai Donthu Mutyalarayudu Badireddy

46,XX gonadal dysgenesis is a rare genetically heterogeneous disorder characterized by underdeveloped ovaries with consequent, impuberism, primary amenorrhea, and hypergonadotropic hypogonadism. Mullerian agenesis or Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is characterized by congenital aplasia of the uterus and the upper part (2/3) of the vagina in a woman with normal development of sec...

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