Moretti-Ferreira D, Koiffmann C P, Listik M, Setian N, Wajntal A
Department of Genetics, State University of São Paulo, Botucatu, Brazil.
Am J Med Genet. 1993 Jun 15;46(5):555-8. doi: 10.1002/ajmg.1320460519.
We describe 2 unrelated patients, a boy and a girl, with an overgrowth syndrome and the following common characteristics: macrocrania, obesity, ocular abnormalities (retinal coloboma and nystagmus), downward slant of palpebral fissures, mental retardation, and delayed bone maturation. Both cases are of sporadic occurrence with no consanguinity between the parents. We suggest that this syndrome is due to a new autosomal dominant mutation and propose to designate it with the acronym of "MOMO syndrome" (Macrosomia, Obesity, Macrocrania, Ocular anomalities.
我们描述了两名无亲缘关系的患者,一名男孩和一名女孩,他们患有一种过度生长综合征,具有以下共同特征:巨头畸形、肥胖、眼部异常(视网膜缺损和眼球震颤)、睑裂向下倾斜、智力迟钝和骨骼成熟延迟。两例均为散发性病例,父母之间无血缘关系。我们认为这种综合征是由一种新的常染色体显性突变引起的,并建议用首字母缩写“MOMO综合征”(巨大儿、肥胖、巨头畸形、眼部异常)来命名它。