A lethal variant of Netherton syndrome in a large inbred family

• Published in: Archives de pédiatrie : organe officiel de la Société française de pédiatrie 2011-03, Vol.18 (3), p.294-298
• Main Authors: Capri, Y, Vanlieferinghen, P, Boeuf, B, Dechelotte, P, Hovnanian, A, Lecomte, B
• Format: Article
• Language: fre
• Subjects: Consanguinity; Fatal Outcome; Female; Homozygote; Humans; Infant, Newborn; Male; Mutation; Netherton Syndrome - genetics; Proteinase Inhibitory Proteins, Secretory - genetics; Serine Peptidase Inhibitor Kazal-Type 5
• ISSN: 1769-664X
• DOI: 10.1016/j.arcped.2010.12.005

Netherton syndrome is a rare autosomal recessive disorder characterized by the triad of ichthyosiform erythrodermia, typical hair dysplasia, and severe atopic features. The broad range of variable expression of this disease is well described and 20% of complications occur during the neonatal period such as hypernatremic dehydration, electrolyte imbalances, recurrent or severe infections, and failure to thrive. Mutation of the SPINK5 gene has been identified as disease-causing in Netherton syndrome, but the pathophysiology still remains unclear. Almost all SPINK5 mutations result in the absence of the serine-protease inhibitor LEKTI protein in both keratinocytes and lymphocytes. In this study, we report on a severe form of Netherton syndrome observed in three patients within a large inbred Rom family. All of them died in the first months of life despite early treatment. They were found to be homozygous for the c.1431-12G>A SPINK5 gene mutation, which has not been associated with a lethal form of the disease thus far. This family illustrates the extreme phenotype of Netherton disease of neonatal onset. Molecular diagnosis allowed further genetic counseling and prenatal testing during other pregnancies.