【佳学基因检测】GLDC相关的甘氨酸脑病基因检测的可信度?
GLDC相关的甘氨酸脑病(Glycine Encephalopathy, GE),又称为非酮症性高甘氨酸血症(Non-Ketotic Hyperglycinemi...
GLDC相关的甘氨酸脑病(Glycine Encephalopathy, GE),又称为非酮症性高甘氨酸血症(Non-Ketotic Hyperglycinemi...
CLN8相关的神经元蜡质脂褐质沉着症(Neuronal Ceroid Lipofuscinosis, CLN8-Related)是一种罕见的神经退行性疾病...
尼曼匹克病C1/D型(Niemann-Pick Disease, Type C1/D)是一种罕见的遗传性疾病,通常是通过常染色体隐性遗传...
是的,对于IQCB1相关的Leber先天性黑蒙(Leber Congenital Amaurosis, LCA)和老年性洛肯综合征5型(Senior-Loke...
Bardet-Biedl综合征(Bardet-Biedl Syndrome,BBS)是一种罕见的遗传性多系统疾病,主要表现为视网膜变性、肥...
是的,伴有皮质下囊肿的巨脑白质脑病(Megalencephalic Leukoencephalopathy with Subcortical Cysts,MLC)是一种罕...
Walker-Warburg综合征(Walker-Warburg Syndrome,WWS)是一种罕见的、严重的、常染色体隐性遗传的先天性肌肉...
RAG2相关Omenn综合征(Omenn Syndrome, RAG2-Related)是一种罕见的原发性免疫缺陷疾病,由RAG2基因突变引起。...
CHRNG相关多发性翼状胬肉综合征(Multiple Pterygium Syndrome, CHRNG-Related)和埃斯科巴综合征(Escobar Syndrom...
常染色体隐性耳聋77型(Deafness, Autosomal Recessive 77,DFNB77)是一种由遗传突变引起的听力损失类型。针...