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Case of polyhydramnios complicated by Opitz G/BBB syndrome

โœ Scribed by Hiroko Tajima; Hiroaki Itoh; Ayako Mochizuki; Yuki Nakamura; Yukiko Kobayashi; Kyuya Hirai; Kazunao Suzuki; Kazuhiro Sugihara; Akira Ohishi; Takehiko Ohzeki; Naohiro Kanayama


Book ID
109007323
Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
633 KB
Volume
36
Category
Article
ISSN
1341-8076

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Communicated by Nancy B. Spinner Opitz G/BBB Syndrome (OS) is a multiple congenital anomaly disorder characterized by defects along the body midline. The disease is characterized by variable expressivity of signs that include hypertelorism, cleft lip and/or palate, laryngo-tracheo-esophageal abnorma

Opitz G/BBB syndrome: Clinical compariso
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Opitz G/BBB syndrome (0s) was first described in 1969 as two separate disorders, the G syndrome, and the BBB syndrome. Since that time, it has become apparent that the BBB and the G syndromes are in fact a single entity, now named the Opitz G/BBB syndrome. However, our recent molecular genetic mappi