MATERNAL PHENYLALANINE HYDROXYLASE DEFICIENCY DISEASE
\mətˈɜːnə͡l fˌiːna͡ɪlˈalɐnˌa͡ɪn hˈa͡ɪdɹəksˌɪle͡ɪs dɪfˈɪʃənsi dɪzˈiːz], \mətˈɜːnəl fˌiːnaɪlˈalɐnˌaɪn hˈaɪdɹəksˌɪleɪs dɪfˈɪʃənsi dɪzˈiːz], \m_ə_t_ˈɜː_n_əl f_ˌiː_n_aɪ_l_ˈa_l_ɐ_n_ˌaɪ_n h_ˈaɪ_d_ɹ_ə_k_s_ˌɪ_l_eɪ_s d_ɪ_f_ˈɪ_ʃ_ə_n_s_i d_ɪ_z_ˈiː_z]\
Definitions of MATERNAL PHENYLALANINE HYDROXYLASE DEFICIENCY DISEASE
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A maternal condition which occurs in untreated or partially treated phenylketonuric females when they become pregnant. This may result in damage to the fetus, including microcephaly, mental retardation, congenital heart disease, intrauterine growth retardation, and craniofacial abnormalities. (From Am J Med Genet 1997 Mar 3;69 (1):89-95)
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Word of the day
Dopamine Acetyltransferase
- An enzyme that catalyzes the of groups from acetyl-CoA to arylamines. They have wide specificity for aromatic amines, particularly serotonin, and can also catalyze acetyl transfer between arylamines without CoA. EC 2.3.1.5.
Nearby Words
- maternal mortalities
- maternal mortality
- maternal mrna
- maternal nutrition
- maternal patterns of care
- Maternal Phenylalanine Hydroxylase Deficiency Disease
- maternal phenylketonuria
- maternal physiologies
- maternal physiology
- maternal placenta
- maternal quality