Le Merrer M, Verloes A, Narcy P, Briard M L
Clinique de Génétique Médicale, Hôpital Necker-Enfants Malades, Paris.
J Genet Hum. 1988 Jun;36(3):257-64.
We report a family in which Opitz-Frias G syndrome is expressed across 4 generations. The propositus displays hypertelorism, low grade hypospadias, cleft palate and lips and cleft larynx, making the diagnosis of G syndrome very likely. A cousin of his mother discloses similar clefts, vulviform hypospadias, anal imperforation and mental retardation. His clinical appearance fits perfectly the diagnosis of BBB syndrome. A nephew shows ambiguous genitalia and hypertelorism. Authors suggest the lumping of the BBB and the G syndrome.
我们报告了一个家族,其中Opitz-Frias G综合征在四代人中都有表现。先证者表现为眼距过宽、轻度尿道下裂、唇腭裂和喉裂,这使得G综合征的诊断非常可能。他母亲的一个堂兄弟有类似的腭裂、外阴样尿道下裂、肛门闭锁和智力障碍。其临床表现完全符合BBB综合征的诊断。一个侄子表现为生殖器模糊和眼距过宽。作者建议将BBB综合征和G综合征合并。