Hereditary Sensory and Autonomic Neuropathy Type Ie

Also Known As:

Dnmt1-Related Dementia, Deafness, and Sensory Neuropathy; Hereditary Sensory Neuropathy Type Ie; Hereditary Sensory and Autonomic Neuropathy Type 1 with Dementia and Hearing Loss; Hsn Ie; Hsnie

Networked: 1 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Nervous System Diseases: 14178
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Congenital Abnormalities: 25723
  - Nervous System Malformations: 35
    - Hereditary Sensory and Autonomic Neuropathies: 326
      - Hereditary Sensory and Autonomic Neuropathy Type Ie: 1
- Inborn Genetic Diseases: 11939
  - Nervous System Heredodegenerative Disorders: 63
    - Hereditary Sensory and Autonomic Neuropathies: 326
      - Hereditary Sensory and Autonomic Neuropathy Type Ie: 1

Experts

1.	Antelmi, Elena: 1 article (01/2020)
2.	Caporali, Leonardo: 1 article (01/2020)
3.	Cappelletti, Martina: 1 article (01/2020)
4.	Capristo, Mariantonietta: 1 article (01/2020)
5.	Carelli, Valerio: 1 article (01/2020)
6.	Contin, Manuela: 1 article (01/2020)
7.	Del Dotto, Valentina: 1 article (01/2020)
8.	La Morgia, Chiara: 1 article (01/2020)
9.	Liguori, Rocco: 1 article (01/2020)
10.	Loguercio Polosa, Paola: 1 article (01/2020)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Hereditary Sensory and Autonomic Neuropathy Type Ie:

1.	MethyltransferasesIBA 01/01/2020 - "ADCA-DN and HSN-IE are rare neurodegenerative syndromes caused by dominant mutations in the replication foci targeting sequence (RFTS) of the DNA methyltransferase 1 (DNMT1) gene. "
2.	DNA (Deoxyribonucleic Acid)IBA 01/01/2020 - "ADCA-DN and HSN-IE are rare neurodegenerative syndromes caused by dominant mutations in the replication foci targeting sequence (RFTS) of the DNA methyltransferase 1 (DNMT1) gene. "