Literature DB >> 7458366

Trichothiodystrophy: sulfur-deficient brittle hair as a marker for a neuroectodermal symptom complex.

V H Price, R B Odom, W H Ward, F T Jones.   

Abstract

Trichothiodystrophy, or sulfur-deficient brittle hair, is a clinical marker for a neuroectodermal symptom complex that usually features mental and physical retardation and may also include nail dystrophy, lamellar ichthyosis, ocular dysplasia, dental caries, and decreased fertility. Cystine-deficient hair is common to all patients. The hairs from two new patients were studied, and the most distinctive microscopic hair findings were striking bright and dark bands seen with polarizing microscopy using crossed polarizers. To date, all hair samples showing this banding have had an abnormally low sulfur content. Two-dimensional electrophoresis on the two protein fractions of the abnormal hair confirmed that the abnormality is caused by decreased synthesis of high-sulfur matrix proteins. Disturbances of the transport or utilization of sulfur-containing amino acids in other neuroectodermal tissues may be proposed to account for the various disease features in these persons.

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Year:  1980        PMID: 7458366     DOI: 10.1001/archderm.116.12.1375

Source DB:  PubMed          Journal:  Arch Dermatol        ISSN: 0003-987X


  28 in total

1.  Unknown syndrome in sibs: pili torti, growth delay, developmental delay, and mild neurological abnormalities.

Authors:  S K Shapira; A S Neish; B R Pober
Journal:  J Med Genet       Date:  1992-07       Impact factor: 6.318

2.  MRI of a very rare hereditary ectodermal dysplasia: PIBI(D)S.

Authors:  A Peserico; P A Battistella; P Bertoli
Journal:  Neuroradiology       Date:  1992       Impact factor: 2.804

3.  Viscoelastic response of human hair cortex.

Authors:  G Nikiforidis; C Balas; D Tsambaos
Journal:  Med Biol Eng Comput       Date:  1992-01       Impact factor: 2.602

Review 4.  [Hereditary photodermatoses].

Authors:  P Poblete-Gutiérrez; W H C Burgdorf; C Has; M Berneburg; J Frank
Journal:  Hautarzt       Date:  2006-12       Impact factor: 0.751

Review 5.  Trichothiodystrophy: a systematic review of 112 published cases characterises a wide spectrum of clinical manifestations.

Authors:  S Faghri; D Tamura; K H Kraemer; J J Digiovanna
Journal:  J Med Genet       Date:  2008-06-25       Impact factor: 6.318

Review 6.  Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: a complex genotype-phenotype relationship.

Authors:  K H Kraemer; N J Patronas; R Schiffmann; B P Brooks; D Tamura; J J DiGiovanna
Journal:  Neuroscience       Date:  2007-02-01       Impact factor: 3.590

7.  Bi-allelic TARS Mutations Are Associated with Brittle Hair Phenotype.

Authors:  Arjan F Theil; Elena Botta; Anja Raams; Desiree E C Smith; Marisa I Mendes; Giuseppina Caligiuri; Sarah Giachetti; Silvia Bione; Roberta Carriero; Giordano Liberi; Luca Zardoni; Sigrid M A Swagemakers; Gajja S Salomons; Alain Sarasin; Alan Lehmann; Peter J van der Spek; Tomoo Ogi; Jan H J Hoeijmakers; Wim Vermeulen; Donata Orioli
Journal:  Am J Hum Genet       Date:  2019-08-01       Impact factor: 11.025

8.  Trichothiodystrophy, xeroderma pigmentosum and PIBI(D)S syndrome.

Authors:  A Rebora; F Crovato
Journal:  Hum Genet       Date:  1988-01       Impact factor: 4.132

9.  ARCH domain of XPD, an anchoring platform for CAK that conditions TFIIH DNA repair and transcription activities.

Authors:  Wassim Abdulrahman; Izarn Iltis; Laura Radu; Cathy Braun; Anne Maglott-Roth; Christophe Giraudon; Jean-Marc Egly; Arnaud Poterszman
Journal:  Proc Natl Acad Sci U S A       Date:  2013-02-04       Impact factor: 11.205

Review 10.  Diseases associated with defective responses to DNA damage.

Authors:  Mark O'Driscoll
Journal:  Cold Spring Harb Perspect Biol       Date:  2012-12-01       Impact factor: 10.005

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