Krajewska-Walasek M, Gradowska W, Ryzko J, Socha P, Chmielik J, Szapłyko W, Kasprzyk J, Górska B, Szreter M, Wolski J, Rysiewski H, Małunowicz E M, Gregorek H, Michałkiewicz J, Pietraszek E, Szapłyko J
Department of Medical Genetics, Children's Memorial Health Institute, Warsaw, Poland.
Clin Dysmorphol. 1999 Jan;8(1):29-40.
We present here extensive clinical and biochemical data on thirteen SLOS (type I) patients with proven defect in cholesterol biosynthesis for further delineation of the classical SLOS phenotype at different patient ages.
我们在此呈现了13例经证实存在胆固醇生物合成缺陷的Smith-Lemli-Opitz综合征(I型)患者的广泛临床和生化数据,以便在不同患者年龄阶段进一步描绘经典的Smith-Lemli-Opitz综合征表型。