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462 Possible Causes for Autosomal Recessive Inheritance Can Occur

  • Anemia

    Transmittance is autosomal recessive inheritance of abnormal GIF on chromosome arm 11q13.[web.archive.org] Destruction of gastric mucosa can occur from gastrectomy or Helicobacter pylori infection.[web.archive.org]

  • Anxiety Disorder

    recessive mode of inheritance) [ 44 ].[ncbi.nlm.nih.gov] The disease most often presents in childhood (in 60% of cases) but can occur in adults (20% of cases) and sometimes even late in life (aged 60 years).[ncbi.nlm.nih.gov] […] leukodystrophy is due to deficiency of arylsulfatase A, an enzyme encoded by the gene ARSA, giving rise to accumulation of urinary sulfatides (prevalence 1/50,000 to 1/170,000, autosomal[ncbi.nlm.nih.gov]

  • Familial Adenomatous Polyposis

    […] in an autosomal recessive type mutation inheritance.[dovemed.com] In this scenario, the inheritance pattern is autosomal recessive, which means that both chromosomes should possess a genetic defect.[dovemed.com] This mutation is inherited in an autosomal dominant fashion There is a variant form of Familial Adenomatous Polyposis Syndrome that can occur when there are mutations in the[dovemed.com]

  • Congenital Deafness

    The following sections explain patterns of inheritance in more detail: Autosomal Recessive Autosomal recessive hearing loss can occur when a child receives a hearing loss[babyhearing.org] Non-Syndromic Hearing Loss : hearing loss that occurs without any other symptoms Syndromic Hearing Loss : hearing loss that occurs with other symptoms of medical importance[babyhearing.org]

  • Joint Subluxation

    Inheritance is autosomal recessive. Scoliosis is secondary to muscle hypotonia and ligament laxity.[ncbi.nlm.nih.gov] Severe progression can occur, and operative treatment is often required. 32 Hypotonia can be very pronounced, leading to gross motor development and loss of ambulation by[ncbi.nlm.nih.gov]

  • Mental Disorder

    recessive mode of inheritance) [ 44 ].[ncbi.nlm.nih.gov] The disease most often presents in childhood (in 60% of cases) but can occur in adults (20% of cases) and sometimes even late in life (aged 60 years).[ncbi.nlm.nih.gov] […] leukodystrophy is due to deficiency of arylsulfatase A, an enzyme encoded by the gene ARSA, giving rise to accumulation of urinary sulfatides (prevalence 1/50,000 to 1/170,000, autosomal[ncbi.nlm.nih.gov]

  • Patent Ductus Arteriosus

    PDA can also be inherited in an autosomal recessive manner.[healthofchildren.com] If a parent has an autosomal dominant form of PDA, there is a 50% chance for each child to have the same or similar condition.[medical-dictionary.thefreedictionary.com] A recessive condition occurs when a child receives two changed or mutated copies of the gene for a particular condition, such as PDA (one copy from each parent).[healthofchildren.com]

  • Retinitis Pigmentosa

    Autosomal recessive inheritance can occur with no known family history of retinitis pigmentosa.[envisionus.com] Nonsyndromic retinitis pigmentosa can be inherited in an autosomal dominant, autosomal recessive, or X-linked manner.[centogene.com] How is retinitis pigmentosa inherited? Autosomal dominant inheritance affects both male and female.[envisionus.com]

  • Muscular Dystrophy

    This can occur due to either inheriting the defect from one's parents or the mutation occurring during early development.[en.wikipedia.org] Disorders may be X-linked recessive, autosomal recessive, or autosomal dominant.[en.wikipedia.org]

  • Carotid Sinus Syncope

    Friedreich ataxia 562, 563 Autosomal recessive inheritance with limb and gait ataxia, bladder dysfunction, and daytime somnolence. Diffuse interstitial fibrosis and HCM.[ahajournals.org] Syncope can be bradycardic or tachycardic. SCD is known to occur. Kearns-Sayre Syndrome 564, 565 Mitochondrial myopathy.[ahajournals.org]

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