HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

monosomy 1p Chromosome 1

Deletion of a portion of the p region of Crhomosome 1. Monosomy 1p36 (OMIM: 607872) is the most common terminal deltion syndrome in humans, occuring in 1 in 5000 births. It causes severe craniofacial abnormalities and developmental disabilities, including delayed growth, CRANIOSYNOSTOSES; MICROCEPHALY; CLEFT PALATE; eye and ear defects; congenital heart defects, seizures, and intellectual disability.
Also Known As:
Chromosome 1, monosomy 1p; Deletion 1p; Monosomy 1p
Networked: 11 relevant articles (1 outcomes, 3 trials/studies)

Relationship Network

Disease Context: Research Results

Related Diseases

1. Meningioma (Meningiomas)
2. Tetraploidy
3. Neoplasms (Cancer)
4. Glioma (Gliomas)
5. Sotos Syndrome

Experts

1. Donato, Annalidia: 1 article (01/2019)
2. Donato, Giuseppe: 1 article (01/2019)
3. Malara, Natalia: 1 article (01/2019)
4. Presta, Ivan: 1 article (01/2019)
5. Vismara, Marco Flavio Michele: 1 article (01/2019)
6. Hu, Huimin: 1 article (02/2016)
7. Jiang, Tao: 1 article (02/2016)
8. Li, Mingyang: 1 article (02/2016)
9. Liu, Yanwei: 1 article (02/2016)
10. Wang, Zheng: 1 article (02/2016)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to monosomy 1p Chromosome 1:
1. Proteins (Proteins, Gene)FDA Link
2. Alkaline PhosphataseIBA
3. Ferritins (Ferritin)IBA
4. EnzymesIBA
5. Biological FactorsIBA
6. Isocitrate Dehydrogenase (Isocitrate Dehydrogenase (NAD+))IBA
7. Glucose (Dextrose)FDA LinkGeneric

Therapies and Procedures

1. Therapeutics
2. Ligation
3. Drug Therapy (Chemotherapy)