CLOUSTONS SYNDROME
\klˈa͡ʊstənz sˈɪndɹə͡ʊm], \klˈaʊstənz sˈɪndɹəʊm], \k_l_ˈaʊ_s_t_ə_n_z s_ˈɪ_n_d_ɹ_əʊ_m]\
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A group of hereditary disorders involving tissues and structures derived from the embryonic ectoderm. They are characterized by the presence of abnormalities at birth and involvement of both the epidermis and skin appendages. They are generally nonprogressive and diffuse. Various forms exist, including anhidrotic and hidrotic dysplasias, FOCAL DERMAL HYPOPLASIA, and aplasia cutis congenita.
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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
- cloudy swelling
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- clouston syndrome
- Cloustons Syndrome
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