Significados de familial cases em inglês

In familial cases, the primary mutation is transmitted in the germ line.

Moreover, in several familial cases, the disease affected young women and children simultaneously.

Analysing only familial cases against all controls, all three loci were significantly associated.

Other possible AURKA germline variants were screened by sequencing 10 of the familial cases.

Scattered familial cases have been found, revealing some genetic variants.

Autosomal dominant inheritance is suggested by the familial cases.

We screened a sample of familial cases of PD for mutation in the alpha-synuclein gene.

Forty-four were sporadic and 29 familial cases.

In several familial cases of AIMAH, specific aberrant hormone receptors are functional in the adrenal of affected members.

We report four familial cases of which three show maternal inheritance, consistent with paternal imprinting of the gene.

These cases have a younger average age of onset of reflux symptoms and diagnosis of EAC than unlikely familial cases.

Comparison of these patients with previous reports suggests that they could represent the first familial cases of the Pitt-Hopkins syndrome.

In the present study the incidence of familial cases was 12.7%.

Results: Familial and sporadic carcinoids are clinically indistinguishable except for the multiple synchronous primary tumors observed in most familial cases.

Approximately fifty percent of all patients are familial cases and the remaining half consists of sporadic cases with no affected parent.

The vast majority of basal cell carcinomas are sporadic tumors, while familial cases associated with certain hereditary syndromes are less common.