KID Syndrome Complicated by Multiple Abscesses of the Parietal Region Skin: Clinical Case
Background. KID syndrome (keratitis-ichthyosis-deafness) is an orphan genetic multisystem disease with autosomal recessive and dominant types of inheritance, it manifests in the neonatal period. The leading triad of symptoms is: skin lesions, ophthalmological diseases and hearing organ pathology. Cl...
| Hlavní autoři: | , , , , |
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| Médium: | Článek |
| Jazyk: | English |
| Vydáno: |
"Paediatrician" Publishers LLC
2021-03-01
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| Edice: | Вопросы современной педиатрии |
| Témata: | |
| On-line přístup: | https://vsp.spr-journal.ru/jour/article/view/2562 |