Keyword Analysis & Research: cohen syndrome


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Keyword CPC PCC Volume Score Length of keyword
cohen syndrome0.08128431814
cohen0.1615315555
syndrome1.610.27618578

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Keyword CPC PCC Volume Score
cohen syndrome1.690.9295681

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  • Cohen syndrome - Genetic and Rare Diseases Information Center

    nih.gov

    https://rarediseases.info.nih.gov/diseases/6126/cohen-syndrome/

    WebCohen syndrome is a congenital (present at birth) condition. Symptoms vary considerably from person to person but may include distinctive facial features, retinal dystrophy, nearsightedness, small head size, intellectual disability, global developmental delay, weak muscle tone, and unusually large range of joint movement.

    DA: 29 PA: 1 MOZ Rank: 65

  • Cohen Syndrome - Symptoms, Causes, Treatment | NORD

    rarediseases.org

    https://rarediseases.org/rare-diseases/cohen-syndrome/

    WebMay 23, 2023 · Disease Overview. Cohen syndrome is a variable genetic disorder characterized by diminished muscle tone (hypotonia), abnormalities of the head, face, hands and feet, eye abnormalities, and non-progressive intellectual disability.

    DA: 30 PA: 82 MOZ Rank: 81

  • Cohen syndrome - Wikipedia

    wikipedia.org

    https://en.wikipedia.org/wiki/Cohen_syndrome

    WebCohen syndrome (also known as Pepper syndrome or Cervenka syndrome) is a very rare autosomal recessive genetic disorder with varied expression, characterised by obesity, intellectual disability, distinct craniofacial abnormalities and potential ocular dysfunction. Signs and symptoms.

    DA: 41 PA: 91 MOZ Rank: 12

  • Cohen syndrome: MedlinePlus Genetics

    medlineplus.gov

    https://medlineplus.gov/genetics/condition/cohen-syndrome/

    WebCohen syndrome is an inherited disorder that is characterized by developmental delay, intellectual disability, small head size (microcephaly), and weak muscle tone (hypotonia). Explore symptoms, inheritance, genetics of this condition.

    DA: 46 PA: 84 MOZ Rank: 72

  • Cohen Syndrome - GeneReviews® - NCBI Bookshelf

    nih.gov

    https://www.ncbi.nlm.nih.gov/books/NBK1482/

    WebAug 29, 2006 · Cohen syndrome is characterized by failure to thrive in infancy and childhood; truncal obesity in the teen years; early-onset hypotonia and developmental delays; microcephaly developing during the first year of life; moderate to profound psychomotor retardation; progressive retinochoroidal dystrophy and high myopia; …

    DA: 37 PA: 73 MOZ Rank: 88


  • Overview - Cohen SyndromeCohen Syndrome

    cohensyndrome.org

    http://www.cohensyndrome.org/overview/

    WebClinical symptoms of Cohen Syndrome are: Failure to thrive in infancy. High myopia and/or retinal dystrophy. Microcephaly. Developmental delay. Joint laxity. Narrow hands and feet and small stature. Friendly disposition. Neutropenia. Characteristic facial features. Early diagnosis and daily life.

    DA: 41 PA: 1 MOZ Rank: 59

  • About: Cohen syndrome

    ncsu.edu

    https://rarediseases.oscar.ncsu.edu/disease/cohen-syndrome/about/

    WebCohen syndrome is an inherited disorder that affects many parts of the body and is characterized by developmental delay, intellectual disability, small head size (microcephaly), and weak muscle tone (hypotonia). Other features common in this condition include worsening nearsightedness (myopia), breakdown (degeneration) of the light-sensitive ...

    DA: 92 PA: 55 MOZ Rank: 8

  • Cohen syndrome – a rare genetic cause of hypotonia in children

    nih.gov

    https://ncbi.nlm.nih.gov/pmc/articles/PMC3150073/

    WebCohen syndrome is a rare, genetic condition, recessively inherited, associated with specific facial dysmorphism, global developmental delay, hypotonia and ophthalmic abnormalities. A delay in making the diagnosis commonly occurs, because of the lack of a definitive molecular test and also because of the clinical variability of the syndrome.

    DA: 63 PA: 19 MOZ Rank: 14

  • Cohen Syndrome | Hereditary Ocular Diseases - University of …

    arizona.edu

    https://disorders.eyes.arizona.edu/disorders/cohen-syndrome

    WebClinical Characteristics. Ocular Features: Patients have early onset night blindness with defective dark adaptation and corresponding ERG abnormalities. Visual fields are constricted peripherally and central visual acuity is variably reduced. A pigmentary retinopathy is often associated with a bull’s eye maculopathy.

    DA: 3 PA: 46 MOZ Rank: 9

  • Cohen Syndrome

    csrfoundation.org

    https://csrfoundation.org/

    WebCohen Syndrome. About. What is Cohen Syndrome? Leadership TeamAdvisors. For Families. Join the Registry. Research. CiitizenCohen Syndrome Working GroupPublicationsPartners.

    DA: 84 PA: 70 MOZ Rank: 28