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  2. List of childhood diseases and disorders - Wikipedia

    en.wikipedia.org/wiki/List_of_childhood_diseases...

    The term childhood disease refers to disease that is contracted or becomes symptomatic before the age of 18 or 21 years old. Many of these diseases can also be contracted by adults. Some childhood diseases include:

  3. Congenital iodine deficiency syndrome - Wikipedia

    en.wikipedia.org/wiki/Congenital_iodine...

    Around the world, the most common cause of congenital iodine deficiency syndrome (endemic cretinism) [1] is dietary iodine deficiency. Iodine is an essential trace element, necessary for the synthesis of thyroid hormones. Iodine deficiency is the most common preventable cause of neonatal and childhood brain damage worldwide. [11]

  4. Myotonia congenita - Wikipedia

    en.wikipedia.org/wiki/Myotonia_congenita

    Myotonia congenita is a congenital neuromuscular channelopathy that affects skeletal muscles (muscles used for movement). It is a genetic disorder.The hallmark of the disease is the failure of initiated contraction to terminate, often referred to as delayed relaxation of the muscles and rigidity. [1]

  5. Childhood chronic illness - Wikipedia

    en.wikipedia.org/wiki/Childhood_chronic_illness

    Chronic diseases in children may have a genetic (hereditary) cause, an environmental (acquired) cause or a combination of both. Early identification and treatment of the disease is key to successful health outcomes. Chronic diseases can affect multiple organ systems and can, therefore, manifest in different ways.

  6. Craniodiaphyseal dysplasia - Wikipedia

    en.wikipedia.org/wiki/Craniodiaphyseal_dysplasia

    Craniodiaphyseal dysplasia (CDD), also known as lionitis, is an extremely rare autosomal recessive bone disorder that causes calcium to build up in the skull, disfiguring the facial features and reducing life expectancy. These calcium deposits decrease the size of cranial foramina, and can decrease the circumference of the cervical spinal canal ...

  7. Oculocerebrorenal syndrome - Wikipedia

    en.wikipedia.org/wiki/Oculocerebrorenal_syndrome

    Oculocerebrorenal syndrome (also called Lowe syndrome) is a rare X-linked recessive disorder characterized by congenital cataracts, hypotonia, intellectual disability, proximal tubular acidosis, aminoaciduria and low-molecular-weight proteinuria.

  8. What to know about nervous system disease 'ataxia' - AOL

    www.aol.com/news/know-nervous-system-disease...

    As a stand-alone condition, "ataxia is a degenerative disease of the nervous system," explains Andrew Rosen, chief executive officer of the National Ataxia Foundation. There are many types ...

  9. Harlequin-type ichthyosis - Wikipedia

    en.wikipedia.org/wiki/Harlequin-type_ichthyosis

    Turner's two children do not have the disease. She died on March 3, 2017, at age 23. [34] Mason van Dyk (born 2013), despite being given a life expectancy of one to five days, was 5 years old as of July 2018. [35]

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