PHENYLALANINE HYDROXYLASE DEFICIENCY DISEASE, MATERNAL
\fˌiːna͡ɪlˈalɐnˌa͡ɪn hˈa͡ɪdɹəksˌɪle͡ɪs dɪfˈɪʃənsi dɪzˈiːz], \fˌiːnaɪlˈalɐnˌaɪn hˈaɪdɹəksˌɪleɪs dɪfˈɪʃənsi dɪzˈiːz], \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 PHENYLALANINE HYDROXYLASE DEFICIENCY DISEASE, MATERNAL
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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
basidiomycota
- comprises fungi bearing the spores on basidium: Gasteromycetes (puffballs); Tiliomycetes (comprising orders Ustilaginales (smuts) and Uredinales (rusts)); Hymenomycetes (mushrooms; toadstools; agarics; bracket fungi); in some classification systems considered a division of kingdom comprises fungi bearing spores on a basidium; includes Gasteromycetes (puffballs) Tiliomycetes comprising the orders Ustilaginales (smuts) and Uredinales (rusts) Hymenomycetes (mushrooms, toadstools, agarics bracket fungi).
Nearby Words
- phenylalanine 4 hydroxylase
- phenylalanine 4 monooxygenase
- phenylalanine ammonia lyase
- phenylalanine hydroxylase
- phenylalanine hydroxylase deficiency disease
- Phenylalanine Hydroxylase Deficiency Disease, Maternal
- phenylalanine hydroxylase deficiency disease, severe
- phenylalanine lysine vasopressin
- phenylalanine mustard
- phenylalanine specific trna
- phenylalanine trna ligase