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Updated: Jul 14, 2026

Genetic Analysis of Hereditary Transthyretin Ala97Ser Related Amyloidosis
Published on: June 9, 2018
[Trichothiodystrophy: PIBIDS syndrome]
R Jiménez-Puya1, J C Moreno-Giménez, F Camacho-Martínez
1Servicio de Dermatología, Hospital Universitario Reina Sofía, Córdoba, España. JIMPUYA@terra.es
Abstract:
Trichothiodystrophy comprises a heterogeneous group of autosomal recessive entities. This fact gives rise to different interrelated neuroectodermal disorders. From a structural point of view these features are the result of the low tissue sulfur content. We report a case of trichothiodystrophy initially classified as Tay syndrome that based on clinical features, complementary exams as well as on the disease evolution was labelled as PIBIDS syndrome.
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