Autosomal sentence example

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

    2
    0
  • To be affected by the disease, which shows autosomal recessive inheritance, a baby must inherit a mutant allele from each parent.

    0
    0
  • To manage autosomal recessive cerebellar ataxia (ARCA) patients in specialist clinics and collect blood samples and clinical data.

    0
    0
  • The risk of a parent with the gene passing the mutation on to a child is 50% (autosomal dominant inheritance ).

    0
    0
  • Autosomal recessive inheritance carries a risk of accompanying learning disabilities.

    0
    0
    Advertisement
  • The pattern of inheritance (the way it is inherited) is called autosomal recessive.

    0
    0
  • Includes X-linked recessive and Autosomal recessive modes of inheritance.

    0
    0
  • While most cases of CJD are sporadic, some are familial, in which case the disease is inherited as an autosomal dominant trait.

    0
    0
  • They can also develop bloat, elbow and hip dysplasia, or autosomal recessive muscular dystrophy.

    0
    0
  • Autosomal refers to the first 22 pairs of chromosomes that are the same in males and females.

    0
    0
    Advertisement
  • In autosomal recessive inheritance, the affected individual has inherited a defective gene from each parent.

    0
    0
  • 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.

    0
    0
  • Kyphoscoliosis type is inherited in an autosomal recessive manner.

    0
    0
  • Arthrochalasia type is inherited in an autosomal dominant manner.

    0
    0
  • Dermatosparaxis type is inherited in an autosomal recessive manner.

    0
    0
    Advertisement
  • Inheritance patterns within this group include X-linked recessive, autosomal dominant, and autosomal recessive.

    0
    0
  • In autosomal dominant EDS, only one copy of a specific gene must be changed for a person to have EDS.

    0
    0
  • In autosomal recessive EDS, both copies of a specific gene must be changed for a person to have EDS.

    0
    0
  • As with autosomal recessive, this implies that both copies of a specific gene must be changed for a person to be affected.

    0
    0
  • In classical autosomal dominant EDS, the risk for recurrence in the parents' other children is one in four.

    0
    0
    Advertisement
  • 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.

    0
    0
  • Most studies suggest that Tourette syndrome is an autosomal dominant disorder with decreased penetrance.

    0
    0
  • An autosomal disorder is one that occurs because of an abnormal gene on a chromosome that is not a sex-linked chromosome.

    0
    0
  • 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.

    0
    0
  • 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.

    0
    0
    Advertisement
  • An autosomal gene is a gene that is located on one of the autosomes or non-sex chromosomes.

    0
    0
  • A person with an autosomal dominant disorder has a 50% chance of passing it to each of their offspring.

    0
    0
  • The inherited form (autosomal recessive) is extremely rare and severe.

    0
    0
  • 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.

    0
    0
  • 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.

    0
    0
    Advertisement
  • Autosomal recessive inheritance means that a person with FMF has mutations in both copies of the MEFV gene.

    0
    0
  • 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.

    0
    0
  • Hereditary hemorrhagic telangiectasia, an autosomal dominant disorder, occurs in one in 50,000 people.

    0
    0
  • 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.

    0
    0
  • All MPS disorder except MPS II are inherited in an autosomal recessive manner.

    0
    0
    Advertisement
  • An individual with an autosomal recessive disorder inherits one non-working genes from each parent.

    0
    0
  • 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.

    0
    0
  • 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.

    0
    0
  • The inheritance pattern appears to be autosomal recessive.

    0
    0
  • In autosomal recessively inherited disorders, a child must inherit two defective genes, one from each parent.

    0
    0
    Advertisement
  • A parent with only one gene for an autosomal recessive disorder does not display symptoms of the disease.

    0
    0
  • Hereditary coproporphyria (HCP) is inherited in an autosomal dominant manner.

    0
    0
  • A person with an autosomal dominant disorder has a 50 percent chance of passing it to each of their offspring.

    0
    0
  • 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.

    0
    0
  • Most, but not all, of these genetic myopathies are inherited through an autosomal dominant pattern of inheritance.

    0
    0
    Advertisement
  • This is called an autosomal recessive pattern of inheritance.

    0
    0
  • Most peroxisomal disorders are inherited autosomal recessive diseases.

    0
    0
  • Autosomal recessive mutation-A pattern of genetic inheritance where two abnormal genes are needed to display the trait or disease.

    0
    0
  • 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.

    0
    0
  • 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.

    0
    0
    Advertisement
  • 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.

    0
    0
  • 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.

    0
    0
  • It is passed from parent to child through an autosomal dominant pattern of inheritance.

    0
    0
  • 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.

    0
    0
  • Nail-patella syndrome is inherited in an autosomal dominant manner.

    0
    0
  • The less common form, autosomal recessive hyper-IgM syndrome (ARHIM), occurs in children who have inherited an abnormal gene from both parents.

    0
    0
  • Such diseases are called autosomal recessive diseases.

    0
    0
  • Such diseases are called autosomal dominant diseases.

    0
    0
  • A severe childhood form is similar in appearance to DMD but is inherited as an autosomal recessive trait.

    0
    0
  • The term autosomal means that the gene for PKU is not located on either the X or Y sex chromosome.

    0
    0
  • The autosomal chromosomes are the nonsex chromosomes.

    0
    0
  • In order for a child to inherit an autosomal recessive abnormality, both parents have to be carriers of the abnormal gene.

    0
    0
  • 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.

    0
    0
  • 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.

    0
    0
  • 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.

    0
    0
  • 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.

    0
    0
  • The autosomal recessive forms of spinal muscular atrophy are the most common inherited cause of infant death.

    0
    0
  • Most of the syndromes are autosomal recessive, meaning that they have no predilection for either sex.

    0
    0
  • Congenital nystagmus may be transmitted genetically, either as an autosomal recessive or dominant, or as an X-linked recessive trait.

    0
    0
  • For example, Leber's amaurosis is an autosomal dominant trait and albinism is X-linked.

    0
    0
  • Type 1 VWD is called an autosomal dominant condition since it is caused by a change in only one vWF gene.

    0
    0
  • 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.

    0
    0
  • 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.

    0
    0
  • 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.

    0
    0
  • 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.

    0
    0
  • 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.

    0
    0
  • Many carriers for the autosomal recessive forms of type 2 VWD and type 3 VWD do not have any symptoms.

    0
    0
  • 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.

    0
    0
  • 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.

    0
    0
  • It results from a child inheriting defective genes from both parents (autosomal recessive pattern of inheritance).

    0
    0
  • Both polydactyly and syndactyly can be caused by the presence of an autosomal dominant trait.

    0
    0
  • An autosomal dominant trait is a gene that is not related to the chromosome that determines gender; therefore, it affects boys and girls equally.

    0
    0
  • Autosomal dominant trait-One of the non-X or non-Y chromosomes that will always express itself when present.

    0
    0
  • In galactosemia, the gene mutation which occurs is inherited in what is known as an autosomal recessive pattern.

    0
    0
  • 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).

    0
    0
  • Achromatopsia, the complete inability to distinguish color, is an autosomal recessive disease of the retina.

    0
    0