Examples of using Autosomal dominant inheritance in English and their translations into Portuguese
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The multiple endocrine neoplasia type 1(men1) is a genetic disorder with autosomal dominant inheritance with high penetrance(near 100% at 50 years) caused by a mutation that inactivates the men1 gene.
transmitted by autosomal dominant inheritance with incomplete penetrance,
Although autosomal dominant inheritance transmission with variable expression and incomplete penetrance is recognized,
Figure 2: Autosomal dominant inheritance- If a person who is a carrier for a dominant altered gene has children, there is a 50% chance of their child inheriting
but it has an autosomal dominant inheritance pattern and progressive evolution
20 degrees and autosomal dominant inheritance pattern with complete penetrance.
suggesting that an autosomal dominant inheritance is most likely10, 11.
only a small fraction of these(4% to 5%) are explained by mutations in high penetrance genes in an autosomal dominant inheritance.
Many families are affected by a familial autosomal dominant inheritance that characterizes the atypical nevus syndrome- melanoma FAM-M.
the remainder follows an autosomal dominant inheritance pattern.
Unna-Thost syndrome is characterized by diffuse non-transgressive palmoplantar keratodermia with an autosomal dominant inheritance pattern and a mutation in the keratin 9 gene.
Hereditary angioedema(hae) is a rare disease with autosomal dominant inheritance, characterized by recurrent attacks of subcutaneous edema,
a disease that has autosomal dominant inheritance i.e., not sex-linked,
In a recent clinical study, it was reported that, in a family comprising 32 individuals, 20 were diagnosed with advanced sleep-phase syndrome as an autosomal dominant inheritance.
their first degree family members since the transmission by autosomal dominant inheritance makes 50% of the family members susceptible.
are monogenic conditions with autosomal dominant inheritance caused by mutations in genes belonging to the same signaling pathway ras-mapk.
studies of familial cases have shown an autosomal dominant inheritance with incomplete penetrance.
is a tumor syndrome with autosomal dominant inheritance, in which tumors are associated with medullary thyroid carcinoma(mtc),
one possible case of mutation due to autosomal dominant inheritance, though the parents do not have the same characteristics.
it deserves attention because several studies have reported a pattern of autosomal dominant inheritance in some individuals, and most of these cases are sporadic.