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Multiple epiphyseal dysplasia (MED), also known as Fairbank's disease, is a rare genetic disorder (dominant form: 1 in 10,000 births) that affects the growing ends of bones. Long bones normally elongate by expansion of cartilage in the growth plate (epiphyseal plate) near their ends.
The majority of neonatal cases (90%) result from applying a vacuum to the head at delivery (ventouse-assisted delivery).The vacuum assist ruptures the emissary veins (i.e., connections between dural sinus and scalp veins) leading to accumulation of blood under the aponeurosis of the scalp muscle and superficial to the periosteum.
The frontal crest of the frontal bone ends below in a small notch which is converted into a foramen, the foramen cecum (or foramen caecum), by articulation with the ethmoid. The foramen cecum varies in size in different subjects, and is frequently impervious; when open, it transmits the emissary vein from the nose to the superior sagittal sinus.
frontal-supraorbital foramen: 2: supraorbital artery supraorbital vein: supraorbital nerve: frontal: anterior cranial fossa: foramen cecum: 1: emissary veins to superior sagittal sinus from the upper part of the nose [3] ethmoid: anterior cranial fossa (osama) foramina of cribriform plate ~20-olfactory nerve bundles (I) ethmoid: anterior ...
Emissary veins have an important role in selective cooling of the head. They also serve as routes where infections are carried into the cranial cavity from the extracranial veins to the intracranial veins. There are several types of emissary veins including the posterior condyloid, mastoid, occipital and parietal emissary veins. [1]
Fibrodysplasia ossificans progressiva (/ ˌ f aɪ b r oʊ d ɪ ˈ s p l eɪ ʒ (i) ə ɒ ˈ s ɪ f ɪ k æ n z p r ə ˈ ɡ r ɛ s ɪ v ə /; [1] abbr. FOP), also called Münchmeyer disease or formerly myositis ossificans progressiva, is an extremely rare connective tissue disease in which fibrous connective tissue such as muscle, tendons, and ligaments turn into bone tissue (ossification).
Swelling appears 2-3 days after birth. If severe the child may develop jaundice, anemia or hypotension. In some cases it may be an indication of a linear skull fracture or be at risk of an infection leading to osteomyelitis or meningitis. The swelling of a cephalohematoma takes weeks to resolve as the blood clot is slowly absorbed from the ...
Cranial sutures. A defining characteristic of Crouzon syndrome is craniosynostosis, which results in an abnormal head shape.This is present in combinations of: frontal bossing, trigonocephaly (fusion of the metopic suture), brachycephaly (fusion of the coronal suture), dolichocephaly (fusion of the sagittal suture), plagiocephaly (unilateral premature closure of lambdoid and coronal sutures ...