When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Leontiasis ossea - Wikipedia

    en.wikipedia.org/wiki/Leontiasis_ossea

    Leontiasis ossea, also known as leontiasis, lion face or lion face syndrome, is a rare medical condition, characterized by an overgrowth of the facial and cranial bones. It is not a disease in itself, but a symptom of other diseases, including Paget's disease , fibrous dysplasia , hyperparathyroidism and renal osteodystrophy .

  3. Roy L. Dennis - Wikipedia

    en.wikipedia.org/wiki/Roy_L._Dennis

    Roy Lee "Rocky" Dennis (December 4, 1961 – October 4, 1978) was an American teenager who had craniodiaphyseal dysplasia, an extremely rare sclerotic bone disorder. The condition usually results in neurological disorders and death during childhood or teenage years.

  4. 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 ...

  5. Pfeiffer syndrome - Wikipedia

    en.wikipedia.org/wiki/Pfeiffer_syndrome

    Pfeiffer syndrome is a rare genetic disorder, characterized by the premature fusion of certain bones of the skull (craniosynostosis), which affects the shape of the head and face. The syndrome includes abnormalities of the hands and feet, such as wide and deviated thumbs and big toes.

  6. Sheinelle Jones' Sudden 'Today' Absence Is Finally Explained

    www.aol.com/sheinelle-jones-sudden-today-absence...

    Today show star Sheinelle Jones is back on air after a brief hiatus, but until recently, fans were unsure as to why she’d been missing.. The co-host of the morning show’s third hour revealed ...

  7. Roberts syndrome - Wikipedia

    en.wikipedia.org/wiki/Roberts_syndrome

    Roberts syndrome, or sometimes called pseudothalidomide syndrome, is an extremely rare autosomal recessive genetic disorder that is characterized by mild to severe prenatal retardation or disruption of cell division, leading to malformation of the bones in the skull, face, arms, and legs. It is caused by a mutation in the ESCO2 gene. It is one ...

  8. Fossil of child with Down syndrome hints at Neanderthal ... - AOL

    www.aol.com/news/fossil-child-down-syndrome...

    Living among a small band of Neanderthals in what is now eastern Spain was a child, perhaps 6 years old, with Down syndrome, as shown in a remarkable fossil preserving traits in the inner ear ...

  9. 'Today' Show Fans Are Reaching Out To Hoda Kotb After ... - AOL

    www.aol.com/today-show-fans-reaching-hoda...

    For premium support please call: 800-290-4726 more ways to reach us