APLASIA CUTIS CONGENITA
\ɐplˈe͡ɪzi͡ə kjˈuːtiz kɒnd͡ʒɪnˈiːtə], \ɐplˈeɪziə kjˈuːtiz kɒndʒɪnˈiːtə], \ɐ_p_l_ˈeɪ_z_iə k_j_ˈuː_t_i_z k_ɒ_n_dʒ_ɪ_n_ˈiː_t_ə]\
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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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