Netherton Syndrome: Considering the Rare in a Nonspecific Presentation.
| Autor: | Brown, Riley H., Morrissette, Summer V., McClees, Sarah F., Huynh, Thy N. |
|---|---|
| Předmět: |
DIAGNOSIS of escherichia coli diseases
GENETIC disorder diagnosis BODY fluid analysis SKIN inflammation diagnosis SKIN disease diagnosis ANEMIA ATOPIC dermatitis CUTANEOUS therapeutics DIFFERENTIAL diagnosis SKIN diseases ERYTHEMA STAPHYLOCOCCAL diseases EXFOLIATIVE dermatitis PSORIASIS DERMATOLOGIC agents RARE diseases INBORN errors of metabolism FLUID therapy BLOOD cell count BILIRUBIN FUNGI TREATMENT effectiveness HYPOCALCEMIA SEBORRHEIC dermatitis CONGENITAL ichthyosiform erythroderma EOSINOPHILIA URINALYSIS BACTERICIDES INFLAMMATION LIVER function tests HYPERNATREMIA DEHYDRATION SYMPTOMS |
| Zdroj: | Journal of the Dermatology Nurses' Association; Sep/Oct2024, Vol. 16 Issue 5, p187-191, 5p |
| Abstrakt: | This case describes a 9-day-old female infant who presented with severe skin peeling and diffuse erythema. As the patient was refractory to standard treatment, a working differential diagnosis was built and included infectious, inflammatory, and inherited etiologies. The patient's workup pointed toward Netherton syndrome, a rare autosomal recessive condition that presents at birth or within the first few weeks of life and is characterized by widespread erythroderma with ichthyosis. [ABSTRACT FROM AUTHOR] |
| Databáze: | Supplemental Index |
| Externí odkaz: |
|