AMELOGENESIS IMPERFECTA
\ɐmˌiːlə͡ʊd͡ʒˈɛnɪsˌɪs ɪmpəfˈɛktə], \ɐmˌiːləʊdʒˈɛnɪsˌɪs ɪmpəfˈɛktə], \ɐ_m_ˌiː_l_əʊ_dʒ_ˈɛ_n_ɪ_s_ˌɪ_s ɪ_m_p_ə_f_ˈɛ_k_t_ə]\
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An autosomal dominant or X-linked disorder in which there is faulty development of the dental enamel owing to agenesis, hypoplasia, or hypocalcification of the enamel. It is marked by enamel that is very thin and friable and frequently stained in various shades of brown. (Dorland, 27th ed)
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Proto Oncogene Proteins c erbB 2
- cell surface protein-tyrosine kinase that is found to be overexpressed in significant number adenocarcinomas. It has extensive homology can heterodimerize EGF EPIDERMAL GROWTH FACTOR), 3 receptor (RECEPTOR, 3) and the 4 receptor. Activation of erbB-2 receptor occurs during heterodimer formation with a ligand-bound erbB family members. EC 2.7.11.-.
Nearby Words
- ameloblastic fibro odontomas
- ameloblastoma
- ameloblastomas
- amelogeneses
- amelogenesis
- Amelogenesis Imperfecta
- amelus
- amen
- amen cadence
- amen corner
- amen-ra