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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2016/06/05 02:33:35」(JST)

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1. 先天性膣奇形の診断およびマネージメント diagnosis and management of congenital anomalies of the vagina
2. 胎児腹部におけるエコーでの腫瘤および石灰化の概要 overview of echogenic masses and calcification in the fetal abdomen
3. 消化管閉鎖症および閉塞の出生前診断 prenatal diagnosis of gastrointestinal atresia and obstruction
4. 純型肺動脈閉鎖症（PA/IVS） pulmonary atresia with intact ventricular septum pa ivs
5. 先天性子宮奇形の外科的マネージメント surgical management of congenital uterine anomalies

Shah K1, Nayak SS2, Shukla A2, Girisha KM2.
Congenital anomalies.Congenit Anom (Kyoto).2016 May;56(3):119-26. doi: 10.1111/cga.12149.
Urorectal septum malformation sequence (URSMS) is a rare spectrum of malformations involving various organ systems. Here, we present eight cases of URSMS, noted in autopsy, with different degrees of complexity, seven being the complete type and one being the partial type. All cases had gastrointesti
PMID 26663027

Spatiotemporal distribution of caudal-type homeobox proteins during development of the hindgut and anorectum in human embryos.

Tang XB1, Zhang T2, Wang WL1, Yuan ZW3, Bai YZ1.
PeerJ.PeerJ.2016 Mar 24;4:e1771. doi: 10.7717/peerj.1771. eCollection 2016.
Background. The objectives of this study were to determine the spatiotemporal distribution of human caudal-type homeobox proteins CDX1, CDX2 and CDX4 during development of the hindgut and anorectum in the embryo and to explore the possible roles of CDX genes during morphogenesis of the hindgut and a
PMID 27042391

Genome-wide association study and meta-analysis identify ISL1 as genome-wide significant susceptibility gene for bladder exstrophy.

Draaken M1, Knapp M2, Pennimpede T3, Schmidt JM4, Ebert AK5, Rösch W6, Stein R7, Utsch B8, Hirsch K9, Boemers TM10, Mangold E4, Heilmann S1, Ludwig KU1, Jenetzky E11, Zwink N12, Moebus S13, Herrmann BG3, Mattheisen M14, Nöthen MM1, Ludwig M15, Reutter H16.
PLoS genetics.PLoS Genet.2015 Mar 12;11(3):e1005024. doi: 10.1371/journal.pgen.1005024. eCollection 2015.
The bladder exstrophy-epispadias complex (BEEC) represents the severe end of the uro-rectal malformation spectrum, and is thought to result from aberrant embryonic morphogenesis of the cloacal membrane and the urorectal septum. The most common form of BEEC is isolated classic bladder exstrophy (CBE)
PMID 25763902

ISP-17-8 Prenatal diagnosis of urorectal septum malformation sequence with the description of new variant : Insight into the embryogenesis(Group 17 Perinatal Care 1,International Session Poster)

P2-61-9 Urorectal septum malformation sequenceに対し,膀胱羊水腔シャントを留置し生児を得た一例(Group 102 胎児異常4,一般演題,第67回学術講演会)

PS-200 部分型Urorectal Septum Malformation Sequenceの1例(泌尿器科疾患,ポスターシンポジウム,病気の子供達に笑顔小児外科に夢そして革新を,第47回日本小児外科学会学術集会)

リンク元	「尿直腸中隔」
関連記事	「septum」

Urorectal septum
	Cloaca of human embryo from twenty-five to twenty-seven days old.
Details
Days	32
Identifiers
Latin	septum urorectale
Code	TE E5.4.9.0.2.0.14
	Anatomical terminology [edit on Wikidata]