Schluth Caroline, Doray Bérénice, Girard-Lemaire Françoise, Kohler Monique, Langer Bruno, Gasser Bernard, Lindner Véronique, Flori Elisabeth
Laboratoire de Cytogénétique, Hôpital de Hautepierre, Strasbourg, France.
Prenat Diagn. 2002 Dec;22(13):1177-80. doi: 10.1002/pd.473.
The 49,XXXXY syndrome is a rare sex chromosome anomaly with an approximate incidence of 1 in 85,000 male live births. The diagnosis is usually ascertained postnatally by the association of mental retardation, variable growth deficiency, Down syndrome-like facial dysmorphy, hypogenitalism and other malformations, especially involving the heart and skeleton. Prenatal diagnosis of the pentasomy 49,XXXXY is generally fortuitous and sonographic features have rarely been described in the literature. We report here on two cases of 49,XXXXY syndrome diagnosed prenatally because of sonographic abnormalities. In the first, amniocentesis was performed at 26 weeks' gestation for polyhydramnios, unilateral clubfoot and micropenis. In the second, a karyotype was carried out on chorionic villi at 13 weeks' gestation for cystic hygroma. These observations and the six previously reported cases demonstrate that cystic hygroma in first or second trimester of pregnancy may be associated with sex chromosome aneuploidy other than Turner syndrome. Moreover, they emphasize the importance of detailed sonographic examination in the second trimester, as small penis and abnormal posturing of the lower extremities are very suggestive of the 49,XXXXY syndrome.
49,XXXXY综合征是一种罕见的性染色体异常疾病,在男性活产儿中的发病率约为1/85000。通常在出生后,根据智力发育迟缓、生长发育迟缓、唐氏综合征样面部畸形、生殖器发育不全及其他畸形(尤其是心脏和骨骼畸形)来确诊。49,XXXXY五体综合征的产前诊断通常是偶然发现的,文献中很少描述其超声特征。我们在此报告两例因超声异常而产前诊断为49,XXXXY综合征的病例。第一例,孕26周时因羊水过多、单侧马蹄内翻足和小阴茎行羊膜腔穿刺术。第二例,孕13周时因颈部水囊瘤对绒毛膜进行核型分析。这些病例及之前报道的六例表明,妊娠早期或中期的颈部水囊瘤可能与除特纳综合征之外的性染色体非整倍体有关。此外,这些病例强调了孕中期详细超声检查的重要性,因为小阴茎和下肢异常姿势非常提示49,XXXXY综合征。