Trichothiodystrophy (TTD) is an autosomal recessive inherited disorder characterised by brittle hair and intellectual impairment. The word breaks down...

syndrome (RTS), Cockayne syndrome (CS), xeroderma pigmentosum (XP), trichothiodystrophy (TTD), combined xeroderma pigmentosum-Cockayne syndrome (XP-CS),...

variety of syndromes; XP, trichothiodystrophy (TTD), or a combination of XP and Cockayne syndrome (XPCS). Both trichothiodystrophy and Cockayne syndrome display...

clues for the diagnosis of trichothiodystrophy. Review of literature reveals extensive associated findings in trichothiodystrophy. Amino acid analyses of...

Mutation in genes ERCC3 (XPB), ERCC2 (XPD) or GTF2H5 (TTDA) cause trichothiodystrophy, a condition characterized by photosensitivity, ichthyosis, brittle...

disorders such as Cockayne syndrome (CS) and trichothiodystrophy (TTD). Cockayne syndrome and trichothiodystrophy are both developmental disorders involving...

RecQ-associated Werner syndrome Bloom syndrome Rothmund–Thomson syndrome NER protein-associated Cockayne syndrome Xeroderma pigmentosum Trichothiodystrophy...

provide information about the known and explored therapeutic targets Trichothiodystrophy, a characteristic of Tay syndrome Trinidad and Tobago dollar, ISO...

Trichorhinophalangeal syndrome type III Trichostasis spinulosa Trichothiodystrophy sun sensitivity Trichothiodystrophy Trichotillomania Tricuspid atresia Tricuspid dysplasia...

Known causes of collodion baby include ichthyosis vulgaris and trichothiodystrophy. Less well documented causes include Sjögren-Larsson syndrome, Netherton...

Syndactyly Syphilis, congenital Teratoma Treacher Collins syndrome Trichothiodystrophy Triple-X syndrome Trisomy 13 Trisomy 9 Turner syndrome Umbilical...

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...

RecQ-associated Werner syndrome Bloom syndrome Rothmund–Thomson syndrome NER protein-associated Cockayne syndrome Xeroderma pigmentosum Trichothiodystrophy...

Menkes' kinky hair syndrome, Netherton's syndrome, hypothyroidism, or trichothiodystrophy. Examination of the hair shafts with a microscope may reveal changes...

Treacher Collins syndrome Trench foot Tricho-hepato-enteric syndrome Trichothiodystrophy Tricho–dento–osseous syndrome Tricho–rhino–phalangeal syndrome Trigeminal...

RecQ-associated Werner syndrome Bloom syndrome Rothmund–Thomson syndrome NER protein-associated Cockayne syndrome Xeroderma pigmentosum Trichothiodystrophy...

RecQ-associated Werner syndrome Bloom syndrome Rothmund–Thomson syndrome NER protein-associated Cockayne syndrome Xeroderma pigmentosum Trichothiodystrophy...

machinery are responsible for multiple genetic disorders including: Trichothiodystrophy (TTD): some individuals are photosensitive, ichthyosis, mental/physical...

screenplay for Baby Doll Tiger tail banding of hair, a symptom of trichothiodystrophy Tiger tail donut, a donut that is twisted with another ingredient...

syndrome Bloom syndrome Cockayne syndrome Xeroderma pigmentosum Trichothiodystrophy Xeroderma pigmentosum-Cockayne syndrome Restrictive dermopathy Mandibuloacral...

RecQ-associated Werner syndrome Bloom syndrome Rothmund–Thomson syndrome NER protein-associated Cockayne syndrome Xeroderma pigmentosum Trichothiodystrophy...

610765 Autosomal recessive ST14 Trichothiodystrophy 601675 Autosomal recessive ERCC2, ERCC3, GTF2H5 Trichothiodystrophy (non-congenital forms) 275550 211390...

RecQ-associated Werner syndrome Bloom syndrome Rothmund–Thomson syndrome NER protein-associated Cockayne syndrome Xeroderma pigmentosum Trichothiodystrophy...

sulfur-deficient brittle hair syndrome, Tay's syndrome, trichothiodystrophy, trichothiodystrophy with ichthyosis) Ichthyosis bullosa of Siemens (ichthyosis...

RecQ-associated Werner syndrome Bloom syndrome Rothmund–Thomson syndrome NER protein-associated Cockayne syndrome Xeroderma pigmentosum Trichothiodystrophy...

syndrome xeroderma pigmentosum complementation group D, photosensitive trichothiodystrophy, and Cockayne syndrome. XPD is essential for the viability of cells...

xeroderma pigmentosum or the noncancer-prone multisystem disorder trichothiodystrophy. Another example in humans is the ERCC6 gene, which encodes a protein...

Nijmegen breakage syndrome, some subgroups of xeroderma pigmentosum, trichothiodystrophy, Fanconi anemia, Bloom syndrome and Rothmund–Thomson syndrome. In...

RecQ-associated Werner syndrome Bloom syndrome Rothmund–Thomson syndrome NER protein-associated Cockayne syndrome Xeroderma pigmentosum Trichothiodystrophy...

with an inherited defect in both alleles of the gene suffer from trichothiodystrophy (TTD), a disease hallmarked by brittle hair and nails and usually...