Autosomal Sentence Examples

The most common mode of inherited deafness is autosomal recessive, which accounts for around 75% of all cases.

To be affected by the disease, which shows autosomal recessive inheritance, a baby must inherit a mutant allele from each parent.

To manage autosomal recessive cerebellar ataxia (ARCA) patients in specialist clinics and collect blood samples and clinical data.

The risk of a parent with the gene passing the mutation on to a child is 50% (autosomal dominant inheritance ).

Autosomal recessive inheritance carries a risk of accompanying learning disabilities.

The pattern of inheritance (the way it is inherited) is called autosomal recessive.

Includes X-linked recessive and Autosomal recessive modes of inheritance.

While most cases of CJD are sporadic, some are familial, in which case the disease is inherited as an autosomal dominant trait.

They can also develop bloat, elbow and hip dysplasia, or autosomal recessive muscular dystrophy.

Autosomal refers to the first 22 pairs of chromosomes that are the same in males and females.

In autosomal recessive inheritance, the affected individual has inherited a defective gene from each parent.

As opposed to autosomal recessive inheritance, only one defective copy of a gene needs to be inherited in order for an individual to develop the disease.

Kyphoscoliosis type is inherited in an autosomal recessive manner.

Arthrochalasia type is inherited in an autosomal dominant manner.

Dermatosparaxis type is inherited in an autosomal recessive manner.

Inheritance patterns within this group include X-linked recessive, autosomal dominant, and autosomal recessive.

In autosomal dominant EDS, only one copy of a specific gene must be changed for a person to have EDS.

In autosomal recessive EDS, both copies of a specific gene must be changed for a person to have EDS.

As with autosomal recessive, this implies that both copies of a specific gene must be changed for a person to be affected.

In classical autosomal dominant EDS, the risk for recurrence in the parents' other children is one in four.

The syndrome is an autosomal dominant disorder, which means that someone who has it has a 50 percent chance of passing it on to any offspring.

Most studies suggest that Tourette syndrome is an autosomal dominant disorder with decreased penetrance.

An autosomal disorder is one that occurs because of an abnormal gene on a chromosome that is not a sex-linked chromosome.

Because in autosomal dominant disorders one gene is abnormal, people with this disorder have about a 50 percent chance of passing the abnormal gene to their offspring.

Autosomal dominant-A pattern of inheritance in which only one of the two copies of an autosomal gene must be abnormal for a genetic condition or disease to occur.

An autosomal gene is a gene that is located on one of the autosomes or non-sex chromosomes.

A person with an autosomal dominant disorder has a 50% chance of passing it to each of their offspring.

The inherited form (autosomal recessive) is extremely rare and severe.

Albinism is a autosomal recessive disease, which means that a person must have two copies of the defective gene to exhibit symptoms of the disease.

The A-T mode of inheritance is autosomal recessive (AR) and requires two copies of the predisposing gene-one from each parent-for the child to have the disease.

Autosomal recessive inheritance means that a person with FMF has mutations in both copies of the MEFV gene.

If both parents carry the same autosomal recessive gene, there is a one in four chance with each pregnancy that the child will inherit both recessive genes and develop FMF.

Hereditary hemorrhagic telangiectasia, an autosomal dominant disorder, occurs in one in 50,000 people.

In this form of SCID the lymphocyte or white blood evaluation is identical to X-linked SCID but is autosomal recessive and, therefore, occurs in girls and boys.

All MPS disorder except MPS II are inherited in an autosomal recessive manner.

An individual with an autosomal recessive disorder inherits one non-working genes from each parent.

When two people are carriers for an autosomal recessive disorder, they have a 25 percent chance with each pregnancy to have a child with the disorder.

However, these children are not at risk to develop the disorder unless the other parent is a carrier or affected with the same autosomal recessive condition.

The inheritance pattern appears to be autosomal recessive.

In autosomal recessively inherited disorders, a child must inherit two defective genes, one from each parent.

A parent with only one gene for an autosomal recessive disorder does not display symptoms of the disease.

Hereditary coproporphyria (HCP) is inherited in an autosomal dominant manner.

A person with an autosomal dominant disorder has a 50 percent chance of passing it to each of their offspring.

Autosomal recessive-A pattern of inheritance in which both copies of an autosomal gene must be abnormal for a genetic condition or disease to occur.

Most, but not all, of these genetic myopathies are inherited through an autosomal dominant pattern of inheritance.

This is called an autosomal recessive pattern of inheritance.

Most peroxisomal disorders are inherited autosomal recessive diseases.

Autosomal recessive mutation-A pattern of genetic inheritance where two abnormal genes are needed to display the trait or disease.

The exact pattern of genetic transmission was not known as of 2004, however; autosomal dominant, autosomal recessive, and sex-linked inheritance patterns have all been studied and rejected.

In autosomal dominant inheritance, a single abnormal gene on one of the autosomal chromosomes (one of the first 22 non-sex chromosomes) from either parent can cause the disease.

If both parents have OI caused by an autosomal dominant gene change, there is a 75 percent chance that the child will inherit one or both OI genes.

Subsequently, however, researchers concluded that the rare recurrence of OI to a couple with a child with autosomal dominant OI is more likely due to gonadal mosaicism.

It is passed from parent to child through an autosomal dominant pattern of inheritance.

In an autosomal dominant pattern of inheritance, only one of these two copies needs to have the mutation (change) or defect in order for the child to have DM.

Nail-patella syndrome is inherited in an autosomal dominant manner.

The less common form, autosomal recessive hyper-IgM syndrome (ARHIM), occurs in children who have inherited an abnormal gene from both parents.

Such diseases are called autosomal recessive diseases.

Such diseases are called autosomal dominant diseases.

A severe childhood form is similar in appearance to DMD but is inherited as an autosomal recessive trait.

The term autosomal means that the gene for PKU is not located on either the X or Y sex chromosome.

The autosomal chromosomes are the nonsex chromosomes.

In order for a child to inherit an autosomal recessive abnormality, both parents have to be carriers of the abnormal gene.

For an autosomal dominant disorder when one parent is a carrier of the abnormal gene, there is a 50 percent chance each child born will inherit the abnormal gene.

As of 2004 the genes causing isolated PDA have not been identified, but it is known that PDA can be inherited through a family in an autosomal dominant pattern or an autosomal recessive pattern.

In an autosomal dominant condition, only one specific changed or mutated copy of the gene for PDA is necessary for a person to have PDA.

If a parent has an autosomal dominant form of PDA, there is a 50 percent chance for each child to have the same or similar condition.

The autosomal recessive forms of spinal muscular atrophy are the most common inherited cause of infant death.

Most of the syndromes are autosomal recessive, meaning that they have no predilection for either sex.

Congenital nystagmus may be transmitted genetically, either as an autosomal recessive or dominant, or as an X-linked recessive trait.

For example, Leber's amaurosis is an autosomal dominant trait and albinism is X-linked.

Type 1 VWD is called an autosomal dominant condition since it is caused by a change in only one vWF gene.

Most cases of type 2 VWD are autosomal dominant since a change in only one vWF gene results in the production of an abnormal form of vWF.

An autosomal dominant form of VWD can be inherited from either parent or can occur as a spontaneous gene mutation (change) in the embryo that is formed when the egg and sperm cells come together during fertilization.

Some cases of type 2 VWD and all cases of type 3 VWD are autosomal recessive, since they are caused only by changes in both vWF genes.

A person with an autosomal recessive form of VWD has inherited both a changed gene from the mother and a changed gene from the father.

Parents who have a child with an autosomal recessive form of VWD are called carriers, since they each possess at least one changed vWF gene.

Many carriers for the autosomal recessive forms of type 2 VWD and type 3 VWD do not have any symptoms.

A person with an autosomal dominant form of VWD has a 50 percent chance of passing the changed gene on to his or her children who may or may not have symptoms.

If one parent has been diagnosed with an autosomal dominant form of VWD or both parents are carriers for an autosomal recessive form of VWD, then prenatal testing should be considered.

It results from a child inheriting defective genes from both parents (autosomal recessive pattern of inheritance).

Both polydactyly and syndactyly can be caused by the presence of an autosomal dominant trait.

An autosomal dominant trait is a gene that is not related to the chromosome that determines gender; therefore, it affects boys and girls equally.

Autosomal dominant trait-One of the non-X or non-Y chromosomes that will always express itself when present.

In galactosemia, the gene mutation which occurs is inherited in what is known as an autosomal recessive pattern.

For persons with a ganglion growth beyond the sigmoid segment of the colon, the inheritance pattern is autosomal dominant with reduced penetrance (risk closer to 50 percent).

Achromatopsia, the complete inability to distinguish color, is an autosomal recessive disease of the retina.