Zannolli R, Mostardini R, Hadjistilianou T, Rosi A, Berardi R, Morgese G
Department of Pediatrics, Policlinico Le Scotte, University of Siena, Italy.
Clin Dysmorphol. 2000 Oct;9(4):281-4. doi: 10.1097/00019605-200009040-00010.
This report describes a 5-year-old girl, mildly mentally retarded, with the following characteristics: macrocephaly; severe obesity; ocular abnormalities (right optic disk coloboma and left choroidal coloboma); short stature; and recurvation of the femur. The case is sporadic with no consanguinity between the parents. The condition was diagnosed tentatively as MOMO syndrome (Macrosomia, Obesity, Macrocephaly, and Ocular Abnormalities) (MIM, 157980), because of the presence of short stature, in contrast with the large stature of the only two previously described cases. It is the third possible example of this rare syndrome to be described in the literature, with some new clinical findings presented.
本报告描述了一名5岁轻度智力发育迟缓的女孩,具有以下特征:巨头畸形;严重肥胖;眼部异常(右眼视盘缺损和左眼脉络膜缺损);身材矮小;以及股骨后弯。该病例为散发性,父母无血缘关系。由于存在身材矮小,与之前仅有的两例报道病例的高大身材不同,该病症初步诊断为MOMO综合征(巨大儿、肥胖、巨头畸形和眼部异常)(MIM,157980)。这是文献中描述的该罕见综合征的第三个可能病例,并呈现了一些新的临床发现。