• Thumbnail for Trichothiodystrophy
    Trichothiodystrophy (TTD) is an autosomal recessive inherited disorder characterised by brittle hair and intellectual impairment. The word breaks down...
    10 KB (1,041 words) - 20:27, 29 October 2024
  • syndrome (RTS), Cockayne syndrome (CS), xeroderma pigmentosum (XP), trichothiodystrophy (TTD), combined xeroderma pigmentosum-Cockayne syndrome (XP-CS),...
    74 KB (8,734 words) - 13:28, 2 November 2024
  • Thumbnail for Xeroderma pigmentosum
    variety of syndromes; XP, trichothiodystrophy (TTD), or a combination of XP and Cockayne syndrome (XPCS). Both trichothiodystrophy and Cockayne syndrome display...
    30 KB (3,013 words) - 19:58, 29 October 2024
  • Thumbnail for Sabinas brittle hair syndrome
    clues for the diagnosis of trichothiodystrophy. Review of literature reveals extensive associated findings in trichothiodystrophy. Amino acid analyses of...
    7 KB (803 words) - 15:23, 23 October 2024
  • Mutation in genes ERCC3 (XPB), ERCC2 (XPD) or GTF2H5 (TTDA) cause trichothiodystrophy, a condition characterized by photosensitivity, ichthyosis, brittle...
    11 KB (1,253 words) - 04:38, 28 October 2024
  • Thumbnail for Helicase
    disorders such as Cockayne syndrome (CS) and trichothiodystrophy (TTD). Cockayne syndrome and trichothiodystrophy are both developmental disorders involving...
    56 KB (6,916 words) - 17:01, 27 August 2024
  • Thumbnail for Werner syndrome
    RecQ-associated Werner syndrome Bloom syndrome Rothmund–Thomson syndrome NER protein-associated Cockayne syndrome Xeroderma pigmentosum Trichothiodystrophy...
    35 KB (4,518 words) - 16:31, 2 November 2024
  • provide information about the known and explored therapeutic targets Trichothiodystrophy, a characteristic of Tay syndrome Trinidad and Tobago dollar, ISO...
    1 KB (175 words) - 11:19, 5 November 2024
  • Thumbnail for Lamellar ichthyosis
    Known causes of collodion baby include ichthyosis vulgaris and trichothiodystrophy. Less well documented causes include Sjögren-Larsson syndrome, Netherton...
    9 KB (975 words) - 17:08, 27 October 2024
  • Syndactyly Syphilis, congenital Teratoma Treacher Collins syndrome Trichothiodystrophy Triple-X syndrome Trisomy 13 Trisomy 9 Turner syndrome Umbilical...
    4 KB (357 words) - 13:01, 28 September 2024
  • Thumbnail for GTF2H5
    In humans, mutation in any one of four genes can give rise to the trichothiodystrophy phenotype. These genes are TTDN1, XPB, XPD and GTF2H5(TTDA). GTF2H5...
    4 KB (529 words) - 00:32, 2 December 2023
  • Trichorhinophalangeal syndrome type III Trichostasis spinulosa Trichothiodystrophy sun sensitivity Trichothiodystrophy Trichotillomania Tricuspid atresia Tricuspid dysplasia...
    10 KB (849 words) - 03:37, 11 January 2024
  • Thumbnail for Bloom syndrome
    RecQ-associated Werner syndrome Bloom syndrome Rothmund–Thomson syndrome NER protein-associated Cockayne syndrome Xeroderma pigmentosum Trichothiodystrophy...
    25 KB (2,759 words) - 19:52, 23 August 2024
  • Thumbnail for Trichorrhexis nodosa
    Menkes' kinky hair syndrome, Netherton's syndrome, hypothyroidism, or trichothiodystrophy. Examination of the hair shafts with a microscope may reveal changes...
    4 KB (357 words) - 14:49, 30 June 2024
  • Treacher Collins syndrome Trench foot Tricho-hepato-enteric syndrome Trichothiodystrophy Tricho–dento–osseous syndrome Tricho–rhino–phalangeal syndrome Trigeminal...
    42 KB (4,068 words) - 16:56, 1 November 2024
  • Thumbnail for Progeria
    RecQ-associated Werner syndrome Bloom syndrome Rothmund–Thomson syndrome NER protein-associated Cockayne syndrome Xeroderma pigmentosum Trichothiodystrophy...
    60 KB (6,225 words) - 02:09, 5 November 2024
  • Thumbnail for Marfanoid–progeroid–lipodystrophy syndrome
    RecQ-associated Werner syndrome Bloom syndrome Rothmund–Thomson syndrome NER protein-associated Cockayne syndrome Xeroderma pigmentosum Trichothiodystrophy...
    8 KB (849 words) - 20:35, 22 July 2023
  • screenplay for Baby Doll Tiger tail banding of hair, a symptom of trichothiodystrophy Tiger tail donut, a donut that is twisted with another ingredient...
    1 KB (206 words) - 19:45, 8 September 2024
  • Thumbnail for Nucleotide excision repair
    machinery are responsible for multiple genetic disorders including: Trichothiodystrophy (TTD): some individuals are photosensitive, ichthyosis, mental/physical...
    33 KB (3,623 words) - 18:02, 20 August 2024
  • RecQ-associated Werner syndrome Bloom syndrome Rothmund–Thomson syndrome NER protein-associated Cockayne syndrome Xeroderma pigmentosum Trichothiodystrophy...
    30 KB (3,089 words) - 08:42, 2 November 2024
  • Thumbnail for Ichthyosis
    610765 Autosomal recessive ST14 Trichothiodystrophy 601675 Autosomal recessive ERCC2, ERCC3, GTF2H5 Trichothiodystrophy (non-congenital forms) 275550 211390...
    14 KB (962 words) - 04:27, 31 October 2024
  • Thumbnail for Cellular senescence
    syndrome Bloom syndrome Cockayne syndrome Xeroderma pigmentosum Trichothiodystrophy Xeroderma pigmentosum-Cockayne syndrome Restrictive dermopathy Mandibuloacral...
    58 KB (6,427 words) - 19:31, 11 July 2024
  • Thumbnail for Dyskeratosis congenita
    RecQ-associated Werner syndrome Bloom syndrome Rothmund–Thomson syndrome NER protein-associated Cockayne syndrome Xeroderma pigmentosum Trichothiodystrophy...
    23 KB (2,629 words) - 09:55, 6 September 2024
  • Thumbnail for List of skin conditions
    sulfur-deficient brittle hair syndrome, Tay's syndrome, trichothiodystrophy, trichothiodystrophy with ichthyosis) Ichthyosis bullosa of Siemens (ichthyosis...
    198 KB (17,956 words) - 10:27, 2 November 2024
  • Thumbnail for Rothmund–Thomson syndrome
    RecQ-associated Werner syndrome Bloom syndrome Rothmund–Thomson syndrome NER protein-associated Cockayne syndrome Xeroderma pigmentosum Trichothiodystrophy...
    10 KB (914 words) - 15:27, 23 October 2024
  • Thumbnail for ERCC2
    syndrome xeroderma pigmentosum complementation group D, photosensitive trichothiodystrophy, and Cockayne syndrome. XPD is essential for the viability of cells...
    15 KB (1,846 words) - 16:57, 27 August 2024
  • Thumbnail for Pleiotropy
    xeroderma pigmentosum or the noncancer-prone multisystem disorder trichothiodystrophy. Another example in humans is the ERCC6 gene, which encodes a protein...
    40 KB (4,786 words) - 14:15, 5 August 2024
  • Nijmegen breakage syndrome, some subgroups of xeroderma pigmentosum, trichothiodystrophy, Fanconi anemia, Bloom syndrome and Rothmund–Thomson syndrome. In...
    97 KB (11,101 words) - 11:45, 3 September 2024
  • Thumbnail for Wiedemann–Rautenstrauch syndrome
    RecQ-associated Werner syndrome Bloom syndrome Rothmund–Thomson syndrome NER protein-associated Cockayne syndrome Xeroderma pigmentosum Trichothiodystrophy...
    8 KB (761 words) - 20:43, 20 August 2024
  • Thumbnail for MPLKIP
    with an inherited defect in both alleles of the gene suffer from trichothiodystrophy (TTD), a disease hallmarked by brittle hair and nails and usually...
    4 KB (578 words) - 05:02, 3 June 2024