Further insights in trichothiodistrophy: a clinical, microscopic, and ultrastructural study of 20 cases and literature review

dc.contributor.author
Ferrando, Juan
dc.contributor.author
Mir-Bonafé, José
dc.contributor.author
Cepeda-Valdés, Rodrigo
dc.contributor.author
Domínguez Ximénez, Anna
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Ocampo-Candiani, Jorge
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García Veigas, Francisco Javier
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Gómez-Flores, Minerva
dc.contributor.author
Salas-Alanis, Julio C.
dc.date.issued
2015-02-26T09:09:27Z
dc.date.issued
2015-02-26T09:09:27Z
dc.date.issued
2012-07-01
dc.date.issued
2015-02-26T09:01:46Z
dc.identifier
0974-7753
dc.identifier
https://hdl.handle.net/2445/63383
dc.identifier
628916
dc.identifier
23180925
dc.description.abstract
Background: Trichothiodistrophy (TTD) is a rare autosomal recessive condition that is characterized by a specific congenital hair shaft dysplasia caused by deficiency of sulfur associated with a wide spectrum of multisystem abnormalities. In this article, we study clinical, microscopic, and ultrastructural findings of 20 patients with TTD with the aim to add further insights regarding to this rare condition. Additionally, analyses of our results are compared with those extracted from the literature in order to enhance its comprehensibility. Materials and Methods: Twenty cases of TTD were included: 7 from Mexico and 14 from Spain. Clinical, microscopic, scanning electron microscopy (SEM) studies and X-ray microanalysis (XrMa) were carried out in all of them. Genetic studies were performed in all seven Mexican cases. Patients with xeroderma pigmentosum and xeroderma pigmentosum/TTD-complex were excluded. Results: Cuticular changes and longitudinal crests of the hair shaft were demonstrated. These crests were irregular, disorganized, following the hair longest axis. Hair shaft sulfur deficiency was disposed discontinuously and intermittently rather than uniformly. This severe decrease of sulfur contents was located close to the trichoschisis areas. Only five patients did not show related disturbances. Micro-dolichocephaly was observed in five cases and represented the most frequent facial dysmorphism found. It is also remarkable that all patients with urologic malformations also combined diverse neurologic disorders. Moreover, three Mexican sisters demonstrated the coexistence of scarce pubic vellus hair, developmental delay, onychodystrophy, and maxillar/mandibullar hypoplasia. Conclusions: TTD phenotype has greatly varied from very subtle forms to severe alterations such as neurologic abnormalities, blindness, lamellar ichthyosis and gonadal malformations. Herein, a multisystem study should be performed mandatorily in patients diagnosed with TTD.
dc.format
6 p.
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application/pdf
dc.language
eng
dc.publisher
Medknow Publications
dc.relation
Reproducció del document publicat a: http://dx.doi.org/10.4103/0974-7753.100075
dc.relation
International Journal of Trichology, 2012, vol. 4, num. 3, p. 158-163
dc.relation
http://dx.doi.org/10.4103/0974-7753.100075
dc.rights
cc by-nc-sa (c) Ferrando et al., 2012
dc.rights
http://creativecommons.org/licenses/by-nc-sa/3.0/
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Medicina)
dc.subject
Malalties rares
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Malalties hereditàries
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Sofre
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Rare diseases
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Genetic diseases
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Sulfur
dc.title
Further insights in trichothiodistrophy: a clinical, microscopic, and ultrastructural study of 20 cases and literature review
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion


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