Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), ISCIII, Madrid, Spain.
Molecular Endocrinology Section, Overgrowth Syndromes Laboratory, Instituto de Genética Médica y Molecular (INGEMM), IdiPAZ, Hospital Universitario la Paz, Universidad Autónoma de Madrid (UAM), Madrid, Spain.
Clin Genet. 2018 Apr;93(4):762-775. doi: 10.1111/cge.13135. Epub 2018 Feb 13.
Smith-Kingsmore syndrome (SKS) OMIM #616638, also known as MINDS syndrome (ORPHA 457485), is a rare autosomal dominant disorder reported so far in 23 patients. SKS is characterized by intellectual disability, macrocephaly/hemi/megalencephaly, and seizures. It is also associated with a pattern of facial dysmorphology and other non-neurological features. Germline or mosaic mutations of the mTOR gene have been detected in all patients. The mTOR gene is a key regulator of cell growth, cell proliferation, protein synthesis and synaptic plasticity, and the mTOR pathway (PI3K-AKT-mTOR) is highly regulated and critical for cell survival and apoptosis. Mutations in different genes in this pathway result in known rare diseases implicated in hemi/megalencephaly with epilepsy, as the tuberous sclerosis complex caused by mutations in TSC1 and TSC2, or the PIK3CA-related overgrowth spectrum (PROS). We here present 4 new cases of SKS, review all clinical and molecular aspects of this disorder, as well as some characteristics of the patients with only brain mTOR somatic mutations.
Smith-Kingsmore 综合征(SKS)(OMIM#616638),也称为 MINDS 综合征(ORPHA 457485),是一种罕见的常染色体显性遗传疾病,迄今为止已在 23 名患者中报道。SKS 的特征是智力障碍、大头畸形/偏侧/巨脑畸形和癫痫发作。它还与面部畸形和其他非神经学特征有关。所有患者均检测到 mTOR 基因突变,包括种系突变或嵌合突变。mTOR 基因是细胞生长、细胞增殖、蛋白质合成和突触可塑性的关键调节剂,mTOR 通路(PI3K-AKT-mTOR)高度调节,对细胞存活和凋亡至关重要。该通路中不同基因的突变导致已知的与偏侧/巨脑畸形伴癫痫的罕见疾病,如 TSC1 和 TSC2 基因突变引起的结节性硬化症,或 PIK3CA 相关过度生长谱(PROS)。我们在此介绍 4 例新的 SKS 病例,回顾该疾病的所有临床和分子方面,以及仅存在大脑 mTOR 体细胞突变的患者的一些特征。