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Single upper central incisor

A hereditary autosomal dominant condition characterized primarily by single (unpaired) deciduous and permanent maxillary central incisors and short stature. Growth hormone deficiencies may also be present. Mutations in the SHH gene have been identified. OMIM: 147250
Also Known As:
Fused incisors; Incisors, Fused; SMMCI Solitary median maxillary central incisor; SMMCI Syndrome; Single central maxillary incisor; Solitary median maxillary central incisor; Solitary median maxillary central incisor syndrome
Networked: 11 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Related Diseases

1. Holoprosencephaly (Arhinencephaly)
2. Microcephaly
3. Kidney Diseases (Kidney Disease)
4. Duane Retraction Syndrome (Duane Syndrome)
5. Coloboma (Colobomas)

Experts

1. Moser, Lorenz: 1 article (07/2021)
2. Schneider, Ute E M: 1 article (07/2021)
3. Attin, Thomas: 1 article (08/2020)
4. Bernardi, Guglielmo: 1 article (08/2020)
5. Bernardi, Sara: 1 article (08/2020)
6. Bianchi, Serena: 1 article (08/2020)
7. Hellwig, Elmar: 1 article (08/2020)
8. Karygianni, Lamprini: 1 article (08/2020)
9. Tchorz, Jörg Philipp: 1 article (08/2020)
10. Ayash, Ghada: 1 article (03/2020)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Single upper central incisor:
1. Growth Hormone (Somatotropin)IBA
2. Indicators and Reagents (Reagents)IBA
3. Intercellular Signaling Peptides and Proteins (Growth Factors)IBA
4. Stainless Steel (Steel, Stainless)IBA
5. Retinaldehyde (Retinal)IBA
6. zirconium oxide (zirconia)IBA

Therapies and Procedures

1. Crowns (Crown, Dental)
2. Orthodontic Space Closure
3. Transplantation
4. Therapeutics