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
Experts
1. | Donato, Annalidia:
1 article
(01/2019)
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2. | Donato, Giuseppe:
1 article
(01/2019)
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3. | Malara, Natalia:
1 article
(01/2019)
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4. | Presta, Ivan:
1 article
(01/2019)
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5. | Vismara, Marco Flavio Michele:
1 article
(01/2019)
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6. | Hu, Huimin:
1 article
(02/2016)
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7. | Jiang, Tao:
1 article
(02/2016)
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8. | Li, Mingyang:
1 article
(02/2016)
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9. | Liu, Yanwei:
1 article
(02/2016)
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10. | Wang, Zheng:
1 article
(02/2016)
|
Drugs and Biologics
Drugs and Important Biological Agents (IBA) related to monosomy 1p Chromosome 1:
Therapies and Procedures