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  2. Crouzon syndrome - Wikipedia

    en.wikipedia.org/wiki/Crouzon_syndrome

    Medical genetics. Crouzon syndrome is an autosomal dominant genetic disorder known as a branchial arch syndrome. Specifically, this syndrome affects the first branchial (or pharyngeal) arch, which is the precursor of the maxilla and mandible. Because the branchial arches are important developmental features in a growing embryo, disturbances in ...

  3. Chromosome 5 - Wikipedia

    en.wikipedia.org/wiki/Chromosome_5

    Chromosome 5 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 5 spans about 182 million base pairs (the building blocks of DNA) and represents almost 6% of the total DNA in cells. Chromosome 5 is the 5th largest human chromosome, yet has one of the lowest gene densities.

  4. Crouzonodermoskeletal syndrome - Wikipedia

    en.wikipedia.org/wiki/Crouzonodermoskeletal_syndrome

    People with Crouzonodermoskeletal syndrome have acanthosis nigricans, a skin condition characterized by thick, dark, velvety skin in body folds and creases, including the neck and underarms. In addition, subtle changes may be seen in the bones of the spine ( vertebrae ). Noncancerous growths called cementomas may develop in the jaw during young ...

  5. Hearing loss with craniofacial syndromes - Wikipedia

    en.wikipedia.org/wiki/Hearing_loss_with...

    Literature has suggested that persons with Crouzon syndrome typically have conductive hearing loss caused by middle ear effusion (or fluid in the middle ear) and perforation to ossicular fixation (ossicles), intratympanic bony masses (tympanic membrane), ossicular anomalies and closure of the oval window. Patients with a sensorineural hearing ...

  6. Chromosome abnormality - Wikipedia

    en.wikipedia.org/wiki/Chromosome_abnormality

    Chromosome abnormality. A chromosomal abnormality, chromosomal anomaly, chromosomal aberration, chromosomal mutation, or chromosomal disorder is a missing, extra, or irregular portion of chromosomal DNA. [1][2] These can occur in the form of numerical abnormalities, where there is an atypical number of chromosomes, or as structural ...

  7. Run (2020 American film) - Wikipedia

    en.wikipedia.org/wiki/Run_(2020_American_film)

    Run (referred to on-screen as Run.) is a 2020 American psychological horror thriller film directed by Aneesh Chaganty, and written by Chaganty and Sev Ohanian.The film stars Kiera Allen as disabled teenager Chloe Sherman, who begins to suspect that her mother, Diane (Sarah Paulson), has been keeping a dark secret about her upbringing.

  8. Missing (1982 film) - Wikipedia

    en.wikipedia.org/wiki/Missing_(1982_film)

    Missing (stylized as missing.) is a 1982 American biographical thriller drama film directed by Costa-Gavras from a screenplay written by Gavras and Donald E. Stewart, adapted from the book The Execution of Charles Horman: An American Sacrifice (1978) by Thomas Hauser (later republished under the title Missing in 1982), based on the disappearance of American journalist Charles Horman, in the ...

  9. Chromosome 10 - Wikipedia

    en.wikipedia.org/wiki/Chromosome_10

    CM000672 (FASTA) Chromosome 10 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 10 spans about 134 million base pairs (the building material of DNA) and represents between 4 and 4.5 percent of the total DNA in cells.