Xeroderma, xerosis or xerosis cutis, or simply dry skin, is a skin condition characterized by excessively dry skin. The term derives from Greek ξηρός...

Xeroderma pigmentosum (XP) is a genetic disorder in which there is a decreased ability to repair DNA damage such as that caused by ultraviolet (UV) light...

hereditary Xeroderma Xeroderma pigmentosum Xeroderma pigmentosum, type 1 Xeroderma pigmentosum, type 2 Xeroderma pigmentosum, type 3 Xeroderma pigmentosum...

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

diseases caused by lack of or malfunctioning of DNA ligase is as follows. Xeroderma pigmentosum, which is commonly known as XP, is an inherited condition...

damage. Xpa mutant individuals often show the severe clinical symptoms of xeroderma pigmentosum, a condition involving extreme sensitivity to sunlight and...

Vitamin A deficiency (VAD) or hypovitaminosis A is a lack of vitamin A in blood and tissues. It is common in poorer countries, especially among children...

gene can result in three different disorders: the cancer-prone syndrome xeroderma pigmentosum complementation group D, photosensitive trichothiodystrophy...

XPB (xeroderma pigmentosum type B) is an ATP-dependent DNA helicase in humans that is a part of the TFIIH transcription factor complex. The 3D-structure...

of defects can result in other rare autosomal recessive diseases like xeroderma pigmentosum and Cockayne syndrome. Currently, mutations in four genes...

of porphyria are aggravated by sunlight. A rare hereditary condition xeroderma pigmentosum (a defect in DNA repair) is thought to increase the risk of...

MUTYH-associated polyposis, Rothmund–Thomson syndrome, Werner syndrome and Xeroderma pigmentosum. Although cancer syndromes exhibit an increased risk of cancer...

complexity Xanthelasma palpebrarum, a cholesterol deposit in the eyelid Xeroderma pigmentosum, a genetic disorder Ilford XP, a chromogenic black and white...

Schwarzenegger, and Rob Riggle. The story is about a teenaged girl with xeroderma pigmentosum (XP), a medical condition which prevents her from going out...

Atypical fibroxanthoma has also been associated with P53 mutations, xeroderma pigmentosum, radiation therapy, trauma, and immunosuppression. Because...

Degenerative disease Genetic disorder Life extension Progeria Senescence Xeroderma pigmentosum List of cutaneous conditions Progeroid syndrome James, William;...

diseases that result from in-born genetic mutations of NER proteins. Xeroderma pigmentosum and Cockayne's syndrome are two examples of NER associated...

expression of the various characteristics of ATR-X in different patients. XPD (Xeroderma pigmentosum factor D, also known as protein ERCC2) is a 5'-3', Superfamily...

development of cancers. An example of such a hereditary cancer syndrome is xeroderma pigmentosum, which causes the development of skin cancers in response...

function are at greater risk. A number of rare genetic conditions, such as xeroderma pigmentosum, also increase the risk. Diagnosis is by biopsy and analysis...

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

X-linked recessive ichthyosis) X-linked recessive chondrodysplasia punctata Xeroderma pigmentosum (Cockayne syndrome complex) XXYY genotype Zimmermann–Laband...

III will live into adulthood. Xeroderma pigmentosum-Cockayne syndrome (XP-CS) occurs when an individual also has xeroderma pigmentosum, another DNA repair...

in XPG. The amino acid linking the N- and I-regions are not conserved. Xeroderma pigmentosum (XP) is a human autosomal recessive disease, characterised...

"accelerated aging diseases", such as Werner syndrome, Cockayne syndrome, or xeroderma pigmentosum, progeria may not be directly caused by defective DNA repair...

The surface of the knuckles of a hand with xeroderma, showing skin cracking (generalized skin fissuring)....

(dérma, dérmatos), skin, human skin dermatology, epidermis, hypodermic, xeroderma -desis binding Greek δέσις (désis) arthrodesis dextr(o)- right, on the...

ATR-Seckel syndrome, MCPH1-dependent primary microcephaly disorder, xeroderma pigmentosum complementation group A deficiency, Fanconi anemia, ligase...

Xeroderma pigmentosum, complementation group C, also known as XPC, is a protein which in humans is encoded by the XPC gene. XPC is involved in the recognition...

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