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Rare congenital genitourinary anomal...
~
Fahmy, Mohamed A. Baky.
Rare congenital genitourinary anomalies[electronic resource] :an illustrated reference guide /
紀錄類型:
書目-語言資料,印刷品 : Monograph/item
杜威分類號:
616.6
書名/作者:
Rare congenital genitourinary anomalies : an illustrated reference guide // by Mohamed A. Baky Fahmy.
作者:
Fahmy, Mohamed A. Baky.
出版者:
Berlin, Heidelberg : : Springer Berlin Heidelberg :, 2015.
面頁冊數:
xvi, 235 p. : : ill., digital ;; 24 cm.
Contained By:
Springer eBooks
標題:
Genitourinary organs - Abnormalities.
標題:
Medicine & Public Health.
標題:
Surgery.
標題:
Pediatric Surgery.
標題:
Urology/Andrology.
ISBN:
9783662436806 (electronic bk.)
ISBN:
9783662436790 (paper)
內容註:
MALE ANOMALIES: Genital -- Penile Agenesis -- Aphallia -- Penile Duplication, Diphallia -- Microphallus, Micropenis -- Penile Torsion, Lateral Penile Curvature, Penile Deviation -- Penoscrotal Transposition -- Webbed Penis -- Buried Penis, Hidden Penis -- Agenesis Of The Scrotum, Congenital Absence Of The Scrotum -- Ectopic Scrotum -- Accessory Scrotum, Accessory Perineal Scrotum, Splenogonadal Fusion -- Urethral -- Anterior Urethral Valve -- Megalourthera -- Urethral Duplication -- FEMALE ANOMALIES: Labial Adhesion -- Ectopic Labium, Ectopic Labium Majus -- Clitoral Duplication -- Uterovaginal Duplication -- Interlabial Masses -- Urethral Prolapse, Prolapsed Ectopic Ureterocele -- Hydrocolpos -- Hydrometrocolpos -- Sarcoma Botryoides -- Rhabdomyosarcoma -- Periurethral Cyst -- Persistent Urogenital Sinus -- Persistent Cloaca.
摘要、提要註:
Patients with rare diseases, affecting less than 1 in 2000 persons, frequently experience delays or errors in diagnosis, sometimes with tragic consequences. Even after the diagnosis has been established, the quality of health care delivered is often poor. This book, which is both textbook and atlas, covers the full range of rare congenital genitourinary anomalies encountered in males and females, many of which have previously been described only in sporadic case reports. In the case of the more established anomalies, variants are presented. For each anomaly, information is provided on incidence, similar cases, clinical presentation, diagnosis, possible management and outcome. Informative supporting illustrations are presented for each anomaly, and the book will serve as an excellent reference for all pediatricians, urologists and surgeons who are responsible for the care of such patients.
電子資源:
http://dx.doi.org/10.1007/978-3-662-43680-6
Rare congenital genitourinary anomalies[electronic resource] :an illustrated reference guide /
Fahmy, Mohamed A. Baky.
Rare congenital genitourinary anomalies
an illustrated reference guide /[electronic resource] :by Mohamed A. Baky Fahmy. - Berlin, Heidelberg :Springer Berlin Heidelberg :2015. - xvi, 235 p. :ill., digital ;24 cm.
MALE ANOMALIES: Genital -- Penile Agenesis -- Aphallia -- Penile Duplication, Diphallia -- Microphallus, Micropenis -- Penile Torsion, Lateral Penile Curvature, Penile Deviation -- Penoscrotal Transposition -- Webbed Penis -- Buried Penis, Hidden Penis -- Agenesis Of The Scrotum, Congenital Absence Of The Scrotum -- Ectopic Scrotum -- Accessory Scrotum, Accessory Perineal Scrotum, Splenogonadal Fusion -- Urethral -- Anterior Urethral Valve -- Megalourthera -- Urethral Duplication -- FEMALE ANOMALIES: Labial Adhesion -- Ectopic Labium, Ectopic Labium Majus -- Clitoral Duplication -- Uterovaginal Duplication -- Interlabial Masses -- Urethral Prolapse, Prolapsed Ectopic Ureterocele -- Hydrocolpos -- Hydrometrocolpos -- Sarcoma Botryoides -- Rhabdomyosarcoma -- Periurethral Cyst -- Persistent Urogenital Sinus -- Persistent Cloaca.
Patients with rare diseases, affecting less than 1 in 2000 persons, frequently experience delays or errors in diagnosis, sometimes with tragic consequences. Even after the diagnosis has been established, the quality of health care delivered is often poor. This book, which is both textbook and atlas, covers the full range of rare congenital genitourinary anomalies encountered in males and females, many of which have previously been described only in sporadic case reports. In the case of the more established anomalies, variants are presented. For each anomaly, information is provided on incidence, similar cases, clinical presentation, diagnosis, possible management and outcome. Informative supporting illustrations are presented for each anomaly, and the book will serve as an excellent reference for all pediatricians, urologists and surgeons who are responsible for the care of such patients.
ISBN: 9783662436806 (electronic bk.)
Standard No.: 10.1007/978-3-662-43680-6doiSubjects--Topical Terms:
604970
Genitourinary organs
--Abnormalities.
LC Class. No.: RC872
Dewey Class. No.: 616.6
Rare congenital genitourinary anomalies[electronic resource] :an illustrated reference guide /
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MALE ANOMALIES: Genital -- Penile Agenesis -- Aphallia -- Penile Duplication, Diphallia -- Microphallus, Micropenis -- Penile Torsion, Lateral Penile Curvature, Penile Deviation -- Penoscrotal Transposition -- Webbed Penis -- Buried Penis, Hidden Penis -- Agenesis Of The Scrotum, Congenital Absence Of The Scrotum -- Ectopic Scrotum -- Accessory Scrotum, Accessory Perineal Scrotum, Splenogonadal Fusion -- Urethral -- Anterior Urethral Valve -- Megalourthera -- Urethral Duplication -- FEMALE ANOMALIES: Labial Adhesion -- Ectopic Labium, Ectopic Labium Majus -- Clitoral Duplication -- Uterovaginal Duplication -- Interlabial Masses -- Urethral Prolapse, Prolapsed Ectopic Ureterocele -- Hydrocolpos -- Hydrometrocolpos -- Sarcoma Botryoides -- Rhabdomyosarcoma -- Periurethral Cyst -- Persistent Urogenital Sinus -- Persistent Cloaca.
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Patients with rare diseases, affecting less than 1 in 2000 persons, frequently experience delays or errors in diagnosis, sometimes with tragic consequences. Even after the diagnosis has been established, the quality of health care delivered is often poor. This book, which is both textbook and atlas, covers the full range of rare congenital genitourinary anomalies encountered in males and females, many of which have previously been described only in sporadic case reports. In the case of the more established anomalies, variants are presented. For each anomaly, information is provided on incidence, similar cases, clinical presentation, diagnosis, possible management and outcome. Informative supporting illustrations are presented for each anomaly, and the book will serve as an excellent reference for all pediatricians, urologists and surgeons who are responsible for the care of such patients.
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