CONGENITAL ICHTHYOSIFORM ERYTHRODERMAS
\kənd͡ʒˈɛnɪtə͡l ˈɪkθɪˌɒsɪfˌɔːm ˈɜːɹɪθɹˌə͡ʊdəməz], \kəndʒˈɛnɪtəl ˈɪkθɪˌɒsɪfˌɔːm ˈɜːɹɪθɹˌəʊdəməz], \k_ə_n_dʒ_ˈɛ_n_ɪ_t_əl ˈɪ_k_θ_ɪ__ˌɒ_s_ɪ_f_ˌɔː_m ˈɜː_ɹ_ɪ_θ_ɹ_ˌəʊ_d_ə_m_ə_z]\
Sort: Oldest first
-
Designation for several severe forms of ichthyosis, present at birth, that are characterized by hyperkeratotic scaling. Infants may be born encased in a collodion membrane which begins shedding within 24 hours. This is followed in about two weeks by persistent generalized scaling. The forms include bullous (HYPERKERATOSIS, EPIDERMOLYTIC), non-bullous (ICHTHYOSIS, LAMELLAR), wet type, and dry type.
By DataStellar Co., Ltd
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
- congenital hypoplastic anemia
- congenital hypoplastic anemias
- congenital ichthyosiform erythroderma
- congenital ichthyosiform erythroderma, dry type
- congenital ichthyosiform erythroderma, wet type
- Congenital Ichthyosiform Erythrodermas
- congenital immunity
- congenital indifference to pain
- congenital infection, toxoplasma gondii
- congenital insensitivity to pain with anhidrosis
- congenital intracranial arteriovenous malformations