Clinical features of Mayer–Rokitansky–Küster–Haüser syndrome diagnosed at under 16 years old: results from a questionnaire survey conducted on all institutions of pediatric surgery and pediatric urology in Japan

被引:0
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作者
Keisuke Yano
Toshio Harumatsu
Koshiro Sugita
Mitsuru Muto
Takafumi Kawano
Satoshi Ieiri
Masayuki Kubota
机构
[1] Kagoshima University,Department of Pediatric Surgery, Research Field in Medicine and Health Sciences, Medical and Dental Sciences Area, Research and Education Assembly
[2] The Research Project for Rare and Intractable Diseases of the Ministry of Health,Representative of Research Team for the Establishment of Treatment Guidelines for Persistent Cloaca, Cloacal Exstrophy and Mayer‑Rokitansky‑Küster‑Häuser Syndrome for the Prop
[3] Labour and Welfare (MHLW),undefined
来源
关键词
Mayer–Rokitansky–Küster–Häuser syndrome; Anorectal malformation; VACTERL association; Nationwide survey; Children;
D O I
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中图分类号
学科分类号
摘要
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页码:1585 / 1589
页数:4
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  • [1] Clinical features of Mayer-Rokitansky-Kuster-Hauser syndrome diagnosed at under 16 years old: results from a questionnaire survey conducted on all institutions of pediatric surgery and pediatric urology in Japan
    Yano, Keisuke
    Harumatsu, Toshio
    Sugita, Koshiro
    Muto, Mitsuru
    Kawano, Takafumi
    Ieiri, Satoshi
    Kubota, Masayuki
    PEDIATRIC SURGERY INTERNATIONAL, 2022, 38 (11) : 1585 - 1589