केराटोसिस हिंदी उपयोग और उदाहरण

एक अपर्याप्त बायोप्सी को रोमकूपों की भागीदारी के साथ एक्टिनिक केराटोसिस के रूप में पढ़ा जा सकता है।

"" इनमें सोरिएसिस (जीर्ण चर्मरोग जिसमें श्वेत रूसी छोड़नेवाले लाल चकत्ते पड़ जाते हैं), इक्थिआसिस (जिसमें चमड़ी में मछली के छिलकों के समान पपड़ी पड़ जाती है), केराटोसिस (जिसमें चमड़ी सींग के समान कड़ी हो जाती है) इत्यादि प्रमुख हैं।

इनमें सोरिएसिस (जीर्ण चर्मरोग जिसमें श्वेत रूसी छोड़नेवाले लाल चकत्ते पड़ जाते हैं), इक्थिआसिस (जिसमें चमड़ी में मछली के छिलकों के समान पपड़ी पड़ जाती है), केराटोसिस (जिसमें चमड़ी सींग के समान कड़ी हो जाती है) इत्यादि प्रमुख हैं।

केराटोसिस इसके अंग्रेजी अर्थ का उदाहरण

Pseudouridine modifications are also implicated in human diseases such as mitochondrial myopathy and sideroblastic anemia (MLASA) and Dyskeratosis congenita.

Dyskeratosis congenita and Hoyeraal-Hreidarsson syndrome are two rare inherited syndromes caused by mutations in DKC1, the gene encoding for the pseudouridine synthase dyskerin.

Populated places in Balkh Province Dyskeratosis congenita (DKC),also known as Zinsser-Engman-Cole syndrome, is a rare progressive congenital disorder with a highly variable phenotype.

The best characterized form of dyskeratosis congenita is a result of one or more mutations in the long arm of the X chromosome in the gene DKC1.

These three different mutations result in a mild form of dyskeratosis congenita which uniquely follows an autosomal dominant pattern of inheritance.

Homozygous recessive individuals show the symptoms of dyskeratosis congenita in full.

These mutations are also autosomal recessive with three specific single-nucleotide polymorphisms being recognized which result in dyskeratosis congenita.

Dyskeratosis congenita is a disorder of poor telomere maintenance mainly due to a number of gene mutations that give rise to abnormal ribosome function, termed ribosomopathy.

The mainstay of treatment in dyskeratosis congenita is hematopoietic stem cell transplantation, best outcome with sibling donor.

Dyskeratosis Congenita in regards to stem cell transplantation have to be very carefully treated with low intensity radiation/chemo to avoid potentially catastrophic effects of Host versus graft disease and toxicity to other organs affected by short telomeres which makes them very sensitive to any radiation especially the lungs, and liver .

Nearly 80% of the patients of dyskeratosis congenita develop bone marrow failure.

Recent research has used induced pluripotent stem cells to study disease mechanisms in humans, and discovered that the reprogramming of somatic cells restores telomere elongation in dyskeratosis congenita (DKC) cells despite the genetic lesions that affect telomerase.