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x-linked

x-linked

x-linked Sentence Examples

  • This may be particularly important for female relatives on the maternal side of a family where a male baby has an X-linked immunodeficiency.

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  • leukemia cases in the X-linked SCID trial.

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  • Subsequently, five further families have been identified, some of which also include individuals with X-linked mental retardation without infantile spasms 48-52.

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  • ornithine transcarbamylase deficiency shows X-linked inheritance with partial dominant expression in carrier females (Vella et al, 1997 ).

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

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  • RP can be sporadic, autosomal dominant, autosomal recessive or X-linked.

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  • Subsequently, five further families have been identified, some of which also include individuals with X-linked mental retardation without infantile spasms 48-52.

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

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  • RP can be sporadic, autosomal dominant, autosomal recessive or X-linked.

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

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  • There are three patterns of inheritance for EDS: autosomal dominant, autosomal recessive, and X-linked (extremely rare).

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  • In X-linked EDS, a specific gene on the X chromosome must be changed.

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  • The few X-linked forms of EDS fall under the category of X-linked recessive.

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  • However, because males only have one X-chromosome, they are affected if an X-linked recessive EDS gene is changed on their single X-chromosome.

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  • X-linked recessive EDS is accompanied by a slightly more complicated pattern of inheritance.

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  • If a father with an X-linked recessive form of EDS passes a copy of his X chromosome to his children, the sons will be unaffected and the daughters will be carriers.

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  • If a mother is a carrier for an X-linked recessive form of EDS, she may have affected or unaffected sons, or carrier or unaffected daughters, depending on the second sex chromosome inherited from the father.

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  • This condition has an X-linked, recessive pattern of inheritance, meaning that the defective gene is carried on the X chromosome.

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  • X-linked: The most common form of SCID accounts for about half of all cases.

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  • Because this is an X-linked condition, it occurs only in boys.

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  • Children with X-linked SCID have low T-cell and natural killer (NK) cell levels but elevated B-cell levels.

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  • 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.

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  • Unlike the other MPS conditions, MPS II is inherited in an X-linked recessive manner, which means that the gene causing the condition is located on the X chromosome, one of the two sex chromosomes.

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  • X-linked gene-A gene carried on the X chromosome, one of the two sex chromosomes.

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  • X-linked adrenoleukodystrophy (X-ALD), a sex-linked disorder characterized by progressive symptoms that begin as behavioral changes, muscle weakness, and speech difficulties.

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  • The more common of the two, known as X-linked hyper-IgM syndrome (XHIM), is caused by an abnormal gene on the X chromosome and affects only boys.

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  • Dimicoli, S., et al. "Complete Recovery from Cryptosporidium parvum Infection with Gastroenteritis and Sclerosing Cholangitis after Successful Bone Marrow Transplantation in Two Brothers with X-Linked Hyper-IgM Syndrome."

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  • Tomizawa, D., et al. "Allogeneic Hematopoietic Stem Cell Transplantation for Seven Children with X-Linked Hyper-IgM Syndrome: A Single-Center Experience."

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  • A., et al. "The X-Linked Hyper-IgM Syndrome: Clinical and Immunologic Features of 79 Patients."

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  • "X-Linked Immunodeficiency with Hyper IgM." eMedicine, October 4, 2002.

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  • X-linked diseases include DMD, BMD, and EDMD.

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  • Women are not usually affected by X-linked diseases, since they will likely have one unaffected copy between the two chromosomes.

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  • Women carriers of X-linked diseases have a one-in-two chance of passing the flawed gene on to each child born.

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  • X-linked agammaglobulinemia is an inherited disease stemming from a defect on the X chromosome, consequently affecting more males than females.

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  • X-linked hypogammaglobulinemia can occur in combination with growth hormone (GH) deficiency, producing short stature and delayed puberty, primarily in boys but also occurring in girls.

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  • Those that are X-linked occur more in males than females; other immunoglobulin deficiencies occur equally in both sexes.

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  • X-linked agammaglobulinemia is an example of this disease.

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  • The congenital immunodeficiency disorder, Bruton's agammaglobulinemia, also known as X-linked agammaglobulinemia, results in a decrease or absence of B lymphocytes and, therefore, a decreased ability to make antibodies.

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  • The most common form of SCID is X-linked, i.e. the defect is on the X chromosome and, therefore, occurs only in boys.

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  • Bruton's agammaglobulinemia is also known as X-linked agammaglobulinemia (XLA).

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  • This is why diseases associated with X linked genes are usually much more common in boys than in girls.

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  • This form of spinal muscular atrophy only affects men; it is an X-linked recessive disorder, meaning that the defective gene is passed from mother to son.

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

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

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  • WAS is inherited as an X-linked genetic disorder and thus only affects males.

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  • The mild form, X-linked thrombocytopenia, is also caused by mutations in this same gene.

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  • A less severe form of the disease, X-linked thrombocytopenia, affects mainly the platelets.

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