Severe atopic eczema treated by dupilumab in a child with keratitis-ichthyosis-deafness syndrome. 2022

Zhouyang Mi, and Feifei Sun, and Zhenzhen Wang, and Qing Zhao, and Futang Pan, and Xiaoxiao Yan, and Lele Sun, and Xiaofeng Shan, and Gongqi Yu, and Baoqi Yang, and Zhongxiang Shi, and Hong Liu, and Furen Zhang
Binzhou Medical University, Yantai, Shandong, China.

UI MeSH Term Description Entries
D007057 Ichthyosis Any of several generalized skin disorders characterized by dryness, roughness, and scaliness, due to hypertrophy of the stratum corneum epidermis. Most are genetic, but some are acquired, developing in association with other systemic disease or genetic syndrome. Xeroderma,Ichthyoses,Xerodermas
D007634 Keratitis Inflammation of the cornea. Keratitides
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
D003876 Dermatitis, Atopic A chronic inflammatory genetically determined disease of the skin marked by increased ability to form reagin (IgE), with increased susceptibility to allergic rhinitis and asthma, and hereditary disposition to a lowered threshold for pruritus. It is manifested by lichenification, excoriation, and crusting, mainly on the flexural surfaces of the elbow and knee. In infants it is known as infantile eczema. Eczema, Atopic,Eczema, Infantile,Neurodermatitis, Atopic,Neurodermatitis, Disseminated,Atopic Dermatitis,Atopic Eczema,Atopic Neurodermatitis,Disseminated Neurodermatitis,Infantile Eczema
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

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