Travan Laura, Rocca Maria Santa, Buonomo Francesca, Cleva Lisa, Pecile Vanna, De Cunto Angela
Institute for Maternal and Child Health, IRCCS "Burlo Garofolo", Trieste, Italy.
J Investig Med High Impact Case Rep. 2015 Feb 18;3(1):2324709615574949. doi: 10.1177/2324709615574949. eCollection 2015 Jan-Mar.
Chromosomal abnormalities may cause growth failure before or since birth. 9q duplication is reported as a cause of intrauterine growth restriction, mild dysmporphism, and intellectual disabilities. We report a case of a maternally inherited 9q21.31q21.33 duplication causing prenatal and postnatal growth restriction with feeding refusal and mild facial dysmorphisms, prenatally diagnosed by single-nucleotide polymorphism array analysis. Hypothesis of the possible pathogenic mechanisms are discussed.
染色体异常可能在出生前或出生后导致生长发育迟缓。据报道,9q重复是宫内生长受限、轻度畸形和智力障碍的一个原因。我们报告一例由母亲遗传的9q21.31q21.33重复导致的病例,该病例引起产前和产后生长受限、拒食以及轻度面部畸形,通过单核苷酸多态性阵列分析进行产前诊断。文中还讨论了可能的致病机制假说。