Evidence of the high prevalence of neurological disorders in nonsyndromic X‐linked recessive ichthyosis: a retrospective case series

Summary Background X‐linked recessive ichthyosis (XLI) is a relatively common type of ichthyosis caused by a deficiency in the steroid sulfatase (STS) enzyme. It is the only type of ichthyosis that can be both syndromic and nonsyndromic. Typical clinical features include dark‐brown scale of variable...

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Veröffentlicht in:	British journal of dermatology (1951) 2018-10, Vol.179 (4), p.933-939
Hauptverfasser:	Rodrigo‐Nicolás, B., Bueno‐Martínez, E., Martín‐Santiago, A., Cañueto, J., Vicente, A., Torrelo, A., Noguera‐Morel, L., Duat‐Rodríguez, A., Jorge‐Finnigan, C., Palacios‐Álvarez, I., García‐Hernández, J.L., Sebaratnam, D.F., González‐Sarmiento, R., Hernández‐Martín, A.
Format:	Artikel
Sprache:	eng
Schlagworte:	Attention deficit hyperactivity disorder Diagnosis Epilepsy Gene deletion Genetic screening Ichthyosis Neurological diseases Neurological disorders Pruritus Steroid sulfatase
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