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Urorectal septum malformation sequence: Prenatal progression, clinical report, and embryology review

✍ Scribed by Luis F. Escobar; Meadow Heiman; Dawn Zimmer; Holly Careskey

Book ID
101453189
Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
192 KB
Volume
143A
Category
Article
ISSN
1552-4825

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πŸ“œ SIMILAR VOLUMES

Partial urorectal septum malformation se
Partial urorectal septum malformation sequence: A report of 25 cases
✍ Wheeler, Patricia G. ;Weaver, David D. πŸ“‚ Article πŸ“… 2001 πŸ› John Wiley and Sons 🌐 English βš– 168 KB

We have identified 25 cases with what we are calling the partial urorectal septum malformation (URSM) sequence, which were seen in our institution over the past 27 years. The partial URSM sequence is defined as a single perineal/anal opening that drains a common cloaca in combination with an absent

Urorectal septum malformation sequence:
Urorectal septum malformation sequence: Report of thirteen additional cases and review of the literature
✍ Wheeler, Patricia G.; Weaver, David D.; Obeime, Mercy O.; Vance, Gail H.; Bull, πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 43 KB πŸ‘ 2 views

We present the findings of 13 additional cases of the urorectal septum malformation (URSM) sequence, and review the literature. The URSM sequence consists of ambiguous genitalia concurrent with absence of perineal and anal openings. The sex ratio of the 13 new cases was 7 males to 6 females and from