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  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. 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 ...

  4. Craniofacial abnormality - Wikipedia

    en.wikipedia.org/wiki/Craniofacial_abnormality

    Craniofacial abnormalities are congenital musculoskeletal disorders which primarily affect the cranium and facial bones. [1]They are associated with the development of the pharyngeal arches. [2]

  5. Crouzon syndrome - Wikipedia

    en.wikipedia.org/wiki/Crouzon_syndrome

    Without treatment, Crouzon syndrome can cause hearing and vision loss, exposure keratitis or conjunctivitis, drying of the cornea, hydrocephalus, sleep apnea, and breathing problems. [medical citation needed] To move the orbits forward, surgeons expose the skull and orbits and reshape the bone. To treat the midface deficiency, surgeons can move ...

  6. Macrocephaly - Wikipedia

    en.wikipedia.org/wiki/Macrocephaly

    Macrocephaly is a condition in which circumference of the human head is abnormally large. [1] It may be pathological or harmless, and can be a familial genetic characteristic. . People diagnosed with macrocephaly will receive further medical tests to determine whether the syndrome is accompanied by particular disorde

  7. Saethre–Chotzen syndrome - Wikipedia

    en.wikipedia.org/wiki/Saethre–Chotzen_syndrome

    Saethre–Chotzen syndrome (SCS), also known as acrocephalosyndactyly type III, is a rare congenital disorder associated with craniosynostosis (premature closure of one or more of the sutures between the bones of the skull). This affects the shape of the head and face, resulting in a cone-shaped head and an asymmetrical face.

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

    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. Prosopometamorphopsia - Wikipedia

    en.wikipedia.org/wiki/Prosopometamorphopsia

    Prosopometamorphopsia is considered a face hallucination and is included under the umbrella of complex visual hallucinations. [7] Unlike other forms of hallucinations such as peduncular hallucinosis or Charles Bonnet syndrome , prosopometamorphopsia does not predominate at a particular time of day; it is a constant experience. [ 7 ]