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Flat forehead is seen in the following conditions and syndromes: [1] Baller–Gerold syndrome; Cataract–growth hormone deficiency–sensory neuropathy–sensorineural hearing loss–skeletal dysplasia syndrome; COG7 congenital disorder of glycosylation; Craniosynostosis and dental anomalies; Ehlers–Danlos syndrome, musculocontractural type
5 symptoms men over 40 should never ignore. ... the symptoms can progress over time,” says Fernandez. “So, obviously, if there were to be a cardiac problem, catching that early would be better ...
The skin between the fingers and toes may be fused (cutaneous syndactyly). This disorder is also characterized by widely spaced eyes (ocular hypertelorism), an abnormally large head size (macrocephaly), and a high, prominent forehead. Rarely, affected individuals may have more serious medical problems including seizures and developmental delay.
Many people with Stickler syndrome are very nearsighted (described as having high myopia) because of the shape of the eye. People with eye involvement are prone to increased pressure within the eye (ocular hypertension) which could lead to glaucoma and tearing or detachment of the light-sensitive retina of the eye (retinal detachment).
10 effective, expert-backed ways to say goodbye to forehead wrinkles.
The most common symptoms of Williams syndrome are heart defects and unusual facial features. Other symptoms include failure to gain weight appropriately in infancy and low muscle tone. People with WS tend to have widely spaced teeth, a long philtrum, and a flattened nasal bridge. [8] Microcephaly is present in one-third of affected individuals.
Glasses prescribed to correct presbyopia may be simple reading glasses, bifocals, trifocals, or progressive lenses. [4] People over 40 are at risk for developing presbyopia and all people become affected to some degree. [1] An estimated 25% of people (1.8 billion globally) had presbyopia as of 2015. [3]
Widely spaced eyes, prominent forehead, flat skull posterior, bulging eyes, low-set ears, flat or concave face, short thumb, and webbed fingers: FGFR2: Isolated unilateral coronal synostosis: Only malformation is the premature fusion of sutures; If left untreated, can lead to facial asymmetry resembling SCS: FGFR (any) Baller–Gerold syndrome ...