Literature DB >> 9764166

Trichothiodystrophy without associated neuroectodermal defects.

C Peter1, J Tomczok, E Hoting, H Behrendt.   

Abstract

Trichothiodystrophy leading to generalized trichorrhexis nodosa-like hair changes with abnormal hair breakage is described in a 4-year-old girl. A marked deficiency of sulphur and the sulphur-containing amino acid, cystine, was detected in the biochemical analysis of the hair. Further investigation of the hair showed the morphological criteria of trichothiodystrophy. Commonly related symptoms, such as mental retardation, ichthyosis and increased sensitivity to sunlight, were not present in our patient.

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Year:  1998        PMID: 9764166     DOI: 10.1046/j.1365-2133.1998.02331.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN: 0007-0963            Impact factor:   9.302


  2 in total

Review 1.  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

2.  Trichothiodystrophy without Associated Neuroectodermal Features in Two Siblings.

Authors:  Jasleen Kaur; Mala Bhalla; Gurvinder Pal Thami
Journal:  Int J Trichology       Date:  2018 May-Jun
  2 in total

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