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  2. Fragile X syndrome - Wikipedia

    en.wikipedia.org/wiki/Fragile_X_syndrome

    Fragile X syndrome co-occurs with autism in many cases and is a suspected genetic cause of the autism in these cases. [12] [23] This finding has resulted in screening for FMR1 mutation to be considered mandatory in children diagnosed with autism. [12]

  3. Auditory processing disorder - Wikipedia

    en.wikipedia.org/wiki/Auditory_processing_disorder

    Auditory processing disorder (APD) is a neurodevelopmental disorder affecting the way the brain processes sounds. [2] Individuals with APD usually have normal structure and function of the ear, but cannot process the information they hear in the same way as others do, which leads to difficulties in recognizing and interpreting sounds, especially the sounds composing speech.

  4. Sensory processing disorder - Wikipedia

    en.wikipedia.org/wiki/Sensory_processing_disorder

    Sensory processing disorder (SPD), formerly known as sensory integration dysfunction, is a condition in which multisensory input is not adequately processed in order to provide appropriate responses to the demands of the environment.

  5. Low-set ears - Wikipedia

    en.wikipedia.org/wiki/Low-set_ears

    They are present in many congenital conditions. Low-set ears are defined as the outer ears being positioned two or more standard deviations lower than the population average. [ 1 ] Clinically, if the point at which the helix (curved upper part) of the outer ear meets the cranium is at or below the line connecting the inner canthi of eyes (the ...

  6. Autism - Wikipedia

    en.wikipedia.org/wiki/Autism

    Autism spectrum disorder [a] (ASD), or simply autism, is a neurodevelopmental disorder "characterized by persistent deficits in social communication and social interaction across multiple contexts" and "restricted, repetitive patterns of behavior, interests, or activities". [11]

  7. Williams syndrome - Wikipedia

    en.wikipedia.org/wiki/Williams_syndrome

    Williams syndrome (WS), also Williams–Beuren syndrome (WBS), is a genetic disorder that affects many parts of the body. [2] Facial features frequently include a broad forehead, underdeveloped chin, short nose, and full cheeks. [2]

  8. CHARGE syndrome - Wikipedia

    en.wikipedia.org/wiki/CHARGE_syndrome

    CHARGE syndrome (formerly known as CHARGE association) is a rare syndrome caused by a genetic disorder.First described in 1979, the acronym "CHARGE" came into use for newborn children with the congenital features of coloboma of the eye, heart defects, atresia of the nasal choanae, restricted growth or development, genital or urinary abnormalities, and ear abnormalities and deafness. [1]

  9. Preauricular sinus and cyst - Wikipedia

    en.wikipedia.org/wiki/Preauricular_sinus_and_cyst

    Each involves the external ear. The difference between them is that a cyst does not connect with the skin, but a sinus does. [ 3 ] Frequency of preauricular sinus differs depending the population: 0.1–0.9% in the US, 0.9% in the UK, and 4–10% in Asia and parts of Africa.