Atkin syndrome

Also Known As:

Atkin Flaitz Patil Smith syndrome; Atkin-Flaitz syndrome; MRX21; Mental Retardation, X-Linked 21; Mental retardation X-linked Atkin type; Mental retardation X-linked, Atkin type; Mental retardation, X-linked nonspecific, type 1; Mental retardation, X-linked, 21; Mental retardation, X-linked, nonspecific; X-linked mental retardation syndrome, Atkin type

Networked: 2 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Related Diseases

1.	Atkin syndrome
2.	Lafora Disease
3.	Neurodegenerative Diseases (Neurodegenerative Disease)
4.	Intellectual Disability (Idiocy)
5.	Familial encephalopathy with neuroserpin inclusion bodies

Experts

1.	Chen, Yucai: 1 article (01/2021)
2.	Cheng, Hongyi: 1 article (01/2021)
3.	Guo, Miao: 1 article (01/2021)
4.	Luo, Xiaona: 1 article (01/2021)
5.	Sun, Xiaomin: 1 article (01/2021)
6.	Wang, Anqi: 1 article (01/2021)
7.	Wang, Chao: 1 article (01/2021)
8.	Wang, Chunmei: 1 article (01/2021)
9.	Wang, Simei: 1 article (01/2021)
10.	Wang, Yilin: 1 article (01/2021)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Atkin syndrome:

1.	Interleukin-1 Receptor Accessory ProteinIBA 01/01/2021 - "Mental retardation, X-linked 21/34 (MRX21/34), is a rare intellectual disability disease caused by mutations in the IL1RAPL1 (Interleukin-1 Receptor Accessory Protein-Like 1) gene. "
2.	Proteins (Proteins, Gene)FDA Link 01/01/2018 - "Some of these regions are in close proximity to genes encoding essential proteins for neuronal functions and human neurodegenerative disorders such as epm2a (Lafora disease), serpini1 (familial encephalopathy with neuroserpin inclusion bodies) and il1rpl1 (mental retardation, X-linked 21). "