Autosomal

In this case cancer susceptibility is inherited in autosomal dominant manner. ❋ Unknown (2004)

The diagnosis: A potentially fatal genetic disorder called autosomal recessive polycystic kidney disease. ❋ Unknown (2008)

For most people, the genome consists of one pair of sex chromosomes (XX in women and XY in men) and twenty-two pairs of chromosomes called autosomal, plus mitochondrial DNA, which is something of a separate story. ❋ Unknown (2008)

People with untreated and uncontrolled phenylketonuria (an autosomal recessive trait) end up profoundly retarded. ❋ Unknown (2010)

Thornton PS, Satin-Smith MS, Herold K, Glaser B, Chiu KC, Nestorowicz A, et al. Familial hyperinsulinism with apparent autosomal dominant inheritance: clinical and genetic differences from the autosomal recessive variant. [see comments]. ❋ Unknown (2010)

This means that in each pregnancy, the fetus has a 50 percent chance of inheriting the autosomal dominant disorder. ❋ Unknown (2009)

They cite a rate of 1: 100 people (higher in certain groups as you know) and say it's the most common autosomal recessive disease. ❋ Aka TBTAM (2009)

Alagille syndrome is an autosomal dominant disorder, which means someone who carries the Jagged1 gene mutation has a 50 percent chance of passing on that mutation to their child. ❋ Unknown (2009)

Gibbs DL, Rice HE, Farrell JA, Adzick NS, Harrison MR: Familial congenital diaphragmatic hernia: An autosomal recessive syndrome with a poor prognosis. ❋ Unknown (2010)

AR, Kiddoo DA, Canning, DA: Unilateral nephrectomy as palliative therapy in infant with autosomal recessive polycystic kidney disease. ❋ Unknown (2010)

The disorders that mutations in these types of genes cause are called autosomal recessive. ❋ Unknown (2009)

When a normally functional gene can compensate for the other mutated copy of the gene; a person can't be affected by an autosomal recessive condition unless he or she has inherited two copies of the mutated gene, one copy from each of his or her carrier parents. ❋ Unknown (2009)

Laparoscopic renal denervation and nephropexy for autosomal dominant polycystic kidney disease related pain in adolescents. ❋ Unknown (2010)

When a person is carrying a mutation in an autosomal dominant gene, each egg or sperm cell has a 50 percent chance of containing the nonfunctioning gene copy and a 50 percent chance of containing the normal copy of the gene. ❋ Unknown (2009)

This is known as autosomal dominant transmission, so photic sneezing now has the irresistible scientific name of “autosomal-dominant compelling helio-opthalmic outburst,” the acronym for which is, of course, ACHOO. ❋ Ewillett (2009)

If a condition is autosomal dominant, a person who carries one copy of the gene containing a mutation will usually manifest some signs of that condition. ❋ Unknown (2009)

It can test for shared strands of autosomal DNA – meaning any line of ancestry, not just pure matrilineal or patrilineal lines. ❋ Unknown (2010)

When a mutated gene "dominates" over a normally functioning gene; when a person is carrying an autosomal dominant gene, he or she has a 50 percent chance of passing on that mutation to his or her child. ❋ Unknown (2009)

The mutated gene "dominates" over the normally functioning gene, so it is called autosomal dominant. ❋ Unknown (2009)

Alagille syndrome — also known as Alagille-Watson syndrome, syndromic bile duct paucity and arteriohepatic dysplasia — is an autosomal dominant inherited disorder associated with liver, heart, eye and skeletal abnormalities, as well as characteristic facial features. ❋ Unknown (2009)