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An "aquiline" nasal profile From parody nose classification Notes on Noses: "It indicates great decision, considerable Energy, Firmness, Absence of Refinement, and disregard for the bienseances of life". [1] An aquiline nose (also called a Roman nose) is a human nose with a prominent bridge, giving it the appearance of being curved or slightly ...
It is characterized by a prominent forehead, widely spaced eyes, an upturned nose, an underdeveloped mandible, dental hypoplasia, and patulous lips. [1] It can be associated with Williams syndrome and Donohue syndrome (leprechaunism). [2] [3]
The facial features of Marshall Syndrome include a flat midface, the appearance of large eyes, short upturned nose, and a round face. The facial features of Stickler syndrome are less prominent but include a rather long flat face, and depressed nasal bridge.
Nasal bridge is the bony part of the nose, overlying the nasal bones, above the part in blue labeled "Cartilage of Septum". The bridge is between the eyes, and just below them. The lower half of the nose is below the bridge. The nasal bridge is the upper, bony part of the nose, which overlies the nasal bones.
The nose may be small, wide, and upturned. The development of the ears and auditory system may be affected in people with Noonan's syndrome. This can result in low-set ears (in over 90%), backward-rotated ears (over 90%), thick helix (outer rim) of ear (over 90%), incomplete folding of ears, chronic otitis media (ear infections), and hearing loss.
A baby affected by Carpenter syndrome will also display malformations of the face. An individual affected by the syndrome may have broad cheeks, a flat nasal bridge, and a wide upturned nose with abnormally large nasal openings. Their ears will most commonly be low, unevenly set, and malformed in structure.
Small upturned nose; Prognathism; Skeletal features: Shortened limbs (more pronounced in lower limbs) Short stature; Progressive coxa vara; On X ray: Abnormal vertebral bodies (particularly in the lumbar region) Avascular necrosis of the capital femoral epiphyses; Striated metaphyses; Generalized mild osteoporosis; Delayed ossification of the ...
Cornelia de Lange syndrome has a widely varied phenotype, meaning people with the syndrome have varied features and challenges. The typical features of CdLS include thick or long eyebrows, a small nose, small stature, developmental delay, long or smooth philtrum, thin upper lip and downturned mouth. [1]