The face of Non‐photosensitive trichothiodystrophy phenotypic spectrum: A subsequent study on paediatric population

Author:

Pascolini Giulia12ORCID,Lipari Martina3,Gaudioso Federica4,Fania Luca5,Di Zenzo Giovanni6,Didona Biagio1

Affiliation:

1. Genetic Counselling Service Istituto Dermopatico dell'Immacolata, IDI‐IRCCS Rome Italy

2. Rare Skin Diseases Center Istituto Dermopatico dell'Immacolata, IDI‐IRCCS Rome Italy

3. Precision Medicine and Pharmacogenomics Unit Sandro Pertini Hospital Rome Italy

4. Medical Genetics Division Foundation IRCCS Cà Granda Ospedale Maggiore Policlinico Milan Italy

5. Dermatology Clinic Istituto Dermopatico dell'Immacolata, IDI‐IRCCS Rome Italy

6. Molecular and Cell Biology Laboratory Istituto Dermopatico dell'Immacolata, IDI‐IRCCS Rome Italy

Abstract

AbstractBackgroundNon‐photosensitive trichothiodystrophies (TTDs) are a diverse group of genodermatoses within the subset of conditions known as “sulphur‐deficient brittle hair” syndromes. A part of them has only recently been identified, revealing novel causative genes and very rare phenotypes of these genetic skin disorders. At the same time, the molecular basis of previously published and unresolved cases has been revealed through the introduction of innovative genetic techniques. We have previously described the facial phenotype of patients with the Photosensitive form of TTD during childhood. This study marks the beginning of an effort to expand the analysis to include individuals of the same age who do not have photosensitivity.MethodsA total of 26 facial portraits of TTD paediatric patients with Non‐photosensitivity from the literature were analysed using computer‐aided technologies, and their facial features were examined through a detailed clinical review.ResultsDistinct facial features were identified in both Photosensitive and Non‐photosensitive TTDs.ConclusionThe present study has comprehensively elucidated the facial features in TTDs, encompassing the Non‐photosensitive clinical spectrum.

Publisher

Wiley

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4. Protein instability associated with AARS1 and MARS1 mutations causes trichothiodystrophy

5. Diagnosis of Trichothiodystrophy in 2 Siblings

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