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Binder type Maxillonasal dysplasia

Maxillofacial abnormalities characterized by a short nose with a flat bridge, a short columella, an acute nasolabial angle, perialar flatness, a convex upper lip, and a tendency to an ANGLE CLASS III MALOCCLUSION. Critical features of the syndrome appear to be midfacial hypoplasia, lack of anterior nasal spine, and malocclusion. May be hereditary (autosomal recessive) or multifactorial. OMIM: 155050
Also Known As:
Maxillonasal dysplasia, Binder type; Binder syndrome
Networked: 15 relevant articles (1 outcomes, 2 trials/studies)

Relationship Network

Disease Context: Research Results

Related Diseases

1. Lithiasis
2. Vitamin K Deficiency
3. Deafness (Deaf Mutism)
4. Cleft Lip (Harelip)
5. Chondrodysplasia Punctata (Stippled Epiphyses)

Experts

1. Fan, Fei: 2 articles (09/2017 - 11/2016)
2. Lu, Xiaona: 2 articles (09/2017 - 11/2016)
3. Tian, Le: 2 articles (09/2017 - 11/2016)
4. Wang, Huan: 2 articles (09/2017 - 11/2016)
5. You, Jianjun: 2 articles (09/2017 - 11/2016)
6. Zhang, Bo: 2 articles (09/2017 - 11/2016)
7. Barbera, Giorgio: 1 article (01/2021)
8. Della Monaca, Marco: 1 article (01/2021)
9. Nocini, Riccardo: 1 article (01/2021)
10. Priore, Paolo: 1 article (01/2021)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Binder type Maxillonasal dysplasia:
1. Cytidine Diphosphate (CDP)IBA
2. SiliconesIBA
3. Vitamin KFDA Link
4. Growth Hormone (Somatotropin)IBA
5. SolutionsIBA
6. SiliconIBA
7. Phenytoin (Dilantin)FDA LinkGeneric
8. Anticonvulsants (Antiepileptic Drugs)IBA

Therapies and Procedures

1. Transplantation
2. Osteotomy
3. Rhinoplasty
4. Orthognathic Surgery
5. Distraction Osteogenesis