Examples of using Xeroderma in English and their translations into Portuguese
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they have monitored people with the hereditary disease xeroderma pigmentosum see Pesquisa FAPESP, issue no 199.
increasing the epidermal loss of water and provoking xeroderma.
Since pigmented maculae and ephelides in the exposed areas were not predominant, and actinic keratosis, strong photosensitivity and photophobia were not observed, the diagnosis of xeroderma pigmentosum was dismissed.
are related to deficiencies in the ner process, such as xeroderma pigmentosum(xp), cockayne syndrome(cs)
to UV light and resulted in a series of xeroderma pigmentosum the signs and symptoms.
Xeroderma or acquired ichtyosis,
Another possible cause of xeroderma would be nutritional disorders in Aids patients.
pruritus from insect stings, xeroderma, contact dermatitis
urea levels, xeroderma, dialysis time
In relation to xeroderma, of the total sample, 45.7% had this characteristic and, when comparing the groups, a statistically significant association between patients with xeroderma and pruritus p 0.031 was found, a fact confirmed in previous studies.
In xeroderma pigmentosum, there is a deficit in DNA defect repair that increases the risk of malignant skin cancer by more than 1000 times.
Xeroderma can be controlled,
For instance the Xeroderma pigmentosum, results from defects in the system of global repair,
one patient who had xeroderma pigmentosum and lived in a distant
eight were albinism cases; five of them were xeroderma pigmentosum cases; two of them were basal-cell nevus syndrome,
it is important to search for new molecular functions that can be associated to the classical phenotypes of the syndromes caused by mutations in ner genes: xeroderma pigmentosum complementation group a,
Mutations in this protein are associated with the most severe form of XERODERMA PIGMENTOSUM.
Mutations at dna repair genes are associated with rare genetic diseases such as xeroderma pigmentosum(xp), cockayne syndrome(cs) and trichothiodystrophy ttd.
While mutations in xpc predispose to xeroderma pigmentosum, modulations in xpc function may play critical role in the acquisition of uv mutations in sporadic melanomas.
genetic predisposition albinism, xeroderma pigmentosum, epidermodysplasia verruciformis,