ALPORT SYNDROME
\ˈalpɔːt sˈɪndɹə͡ʊm], \ˈalpɔːt sˈɪndɹəʊm], \ˈa_l_p_ɔː_t s_ˈɪ_n_d_ɹ_əʊ_m]\
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Hereditary disease characterized initially by hematuria and slowly progressing to renal insufficiency. It is sometimes associated with perceptual deafness and/or congenital ocular defects.
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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.-.