A case of neonatal Netherton syndrome / 中国当代儿科杂志
Chinese Journal of Contemporary Pediatrics
; (12): 103-106, 2024.
Article
in Zh
| WPRIM
| ID: wpr-1009901
Responsible library:
WPRO
ABSTRACT
A male infant, aged 6 days, was admitted to the hospital due to respiratory distress and systemic desquamative rash after birth. The infant presented with erythema and desquamative rash, respiratory failure, recurrent infections, chronic diarrhea, hypernatremic dehydration, and growth retardation. Comprehensive treatment, including anti-infection therapy, intravenous immunoglobulin administration, and skin care, resulted in improvement of the rash, but recurrent infections persisted. Second-generation sequencing revealed a homozygous mutation in the SPINK5 gene, consistent with the pathogenic variation of Netherton syndrome. The family opted for palliative care, and the infant died at the age of 2 months after discharge. This report documents a case of Netherton syndrome caused by the SPINK5 gene mutation in the neonatal period, and highlights multidisciplinary diagnosis and therapy for this condition.
Key words
Full text:
1
Database:
WPRIM
Main subject:
Dyspnea
/
Exanthema
/
Netherton Syndrome
/
Reinfection
/
Homozygote
Limits:
Humans
/
Infant
/
Male
/
Newborn
Language:
Zh
Journal:
Chinese Journal of Contemporary Pediatrics
Year:
2024
Document type:
Article