Ramelli Gian Paolo, Silacci Charlotte, Ferrarini Alessandra, Cattaneo Claudio, Visconti Paola, Pescia Graziano
Department of Paediatrics, Ospedale San Giovanni, Bellinzona, Switzerland.
Dev Med Child Neurol. 2008 Dec;50(12):953-5. doi: 10.1111/j.1469-8749.2008.03048.x.
Microduplication of the 22q11.2 chromosomal region has been recognized since 1999 and has been associated with a highly variable phenotype. Neurodevelopmental impairment and behavioural problems are very common in patients with 22q11.2 duplication. Autism spectrum disorders (ASDs) have previously been reported in only two patients with 22q11.2 duplication and striking dysmorphic features. We report here on a 4-year-old male of healthy consanguineous parents presenting with ASD according to DSMIV, revised, criteria as a primary manifestation. The child walked at 16 months and started to say one word and some sounds. Parents noticed a subsequent developmental arrest. At 4 years his functional development age, evaluated by the Psychoeducational Profile, was roughly 6 months. Mild non-specific facial dysmorphism was noted. Genetic analyses of the child demonstrated a de novo microduplication of the 22q11.2 chromosomal region. This genetic anomaly was best seen in interphases of blood lymphocytes and in buccal smear nuclei. Our case illustrates once again the clinical heterogeneity of the 22q11.2 duplication as well as the wide genetic complexity of ASD. We suggest that genetic evaluation of ASD should include fluorescence in-situ hybridization analysis of the 22q11.2 chromosomal region.
22q11.2染色体区域的微重复自1999年以来已被认识到,并且与高度可变的表型相关。神经发育障碍和行为问题在22q11.2重复的患者中非常常见。自闭症谱系障碍(ASD)此前仅在两名具有22q11.2重复和明显畸形特征的患者中被报道过。我们在此报告一名4岁男性,其父母为健康近亲,根据修订后的DSMIV标准,该患儿以ASD作为主要表现。患儿16个月时会走路,开始说单个单词和发出一些声音。父母随后注意到其发育停滞。4岁时,通过心理教育概况评估,其功能发育年龄约为6个月。注意到有轻度非特异性面部畸形。对该患儿的基因分析显示22q11.2染色体区域存在新生微重复。这种基因异常在血液淋巴细胞间期和颊黏膜涂片细胞核中最易观察到。我们的病例再次说明了22q11.2重复的临床异质性以及ASD广泛的遗传复杂性。我们建议对ASD的基因评估应包括对22q11.2染色体区域的荧光原位杂交分析。