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  2. Naked foal syndrome - Wikipedia

    en.wikipedia.org/wiki/Naked_foal_syndrome

    Naked foal syndrome (NFS) is a genetic disorder specific to the Akhal-Teke horse breed. A rare genodermatosis , it is characterized by almost complete hairlessness and mild ichthyosis . The condition is inherited as a monogenic autosomal recessive trait, and affected horses typically die between a few weeks and three years of age.

  3. Asphyxiating thoracic dysplasia - Wikipedia

    en.wikipedia.org/wiki/Asphyxiating_thoracic...

    Jeune syndrome is a rare genetic disorder that affects the way a child's cartilage and bones develop. It begins before the child is born and primarily affects the child's rib cage, pelvis, arms and legs. [5] Usually, problems with the rib cage cause the most serious health problems for children with Jeune syndrome.

  4. Mental retardation and microcephaly with pontine and ...

    en.wikipedia.org/wiki/Mental_retardation_and...

    MICPCH in males may occur with or without severe epileptic encephalopathy (Ohtahara syndrome, West syndrome, or early myoclonic epilepsy) in addition to severe-to-profound developmental delay. When seizures are present, they occur early and may be intractable. [7] Prognosis is poor for males with this condition. [8]

  5. I'm About to Turn 73. How Do I Avoid RMD Taxes? - AOL

    www.aol.com/turn-73-avoid-rmd-taxes-140103099.html

    The tables are designed to withdraw all your account assets by the estimated end of your life. If you turn 73 in 2024, your life expectancy would be 26.5 years.

  6. Rhizomelic chondrodysplasia punctata - Wikipedia

    en.wikipedia.org/wiki/Rhizomelic...

    Children with classical, or severe, RCDP1 have severe developmental disabilities. Most of them achieve early developmental skills, such as smiling, but they will not develop skills expected from a baby older than six months (such as feeding themselves or walking). [4] By contrast, children with non-classical mild RCDP1 often learn to walk and ...

  7. Spondylocostal dysostosis - Wikipedia

    en.wikipedia.org/wiki/Spondylocostal_dysostosis

    Spondylocostal dysostosis, also known as Jarcho-Levin syndrome (JLS), is a rare, heritable axial skeleton growth disorder. It is characterized by widespread and sometimes severe malformations of the vertebral column and ribs , shortened thorax , and moderate to severe scoliosis and kyphosis .

  8. Congenital contractural arachnodactyly - Wikipedia

    en.wikipedia.org/wiki/Congenital_contractural_ar...

    Congenital contractural arachnodactyly (CCA), also known as Beals–Hecht syndrome, is a rare autosomal dominant congenital connective tissue disorder. [1] As with Marfan syndrome , people with CCA typically have an arm span that is greater than their height and very long fingers and toes . [ 2 ]

  9. ROHHAD - Wikipedia

    en.wikipedia.org/wiki/ROHHAD

    It has been found that children who are diagnosed earlier in life and, by extension, receive earlier treatment for hypoventilation and hypothalamic dysfunction (fluid imbalances, etc.) are less likely to develop behavioral issues or experience sudden cardiorespiratory arrest later in life.