hypertelorism वाक्य
उदाहरण वाक्य
मोबाइल
- Males are usually more mildly affected, presenting with only hypertelorism.
- Then, the orbits are rotated internally, to correct the hypertelorism.
- Prenatally, various features of FND ( such as hypertelorism ) can be recognized using ultrasound techniques.
- A male child with short stature and hypertelorism could have several different disorders, as these findings are not highly specific.
- Other conditions may also show symptoms of FND . For example, there are other syndromes that also represent with hypertelorism.
- These include hypospadias-dysphagia syndrome, Opitz-Frias syndrome, telecanthus with associated abnormalities, and hypertelorism-hypospadias syndrome.
- Of all the impairments, female carriers of X-linked Type I Opitz G / BBB Syndrome usually only have ocular hypertelorism.
- The shallow eye sockets make the eyes more prominent or bulging and cause the eyes to be more separated than normal ( hypertelorism ).
- FND consists of various nasal malformations that result from excessive tissue in the frontonasal process, which results in hypertelorism and a broad nasal bridge.
- This disorder is also characterized by widely spaced eyes ( ocular hypertelorism ), an abnormally large head size ( macrocephaly ), and a high, prominent forehead.
- Most males have mild symptoms such as hypertelorism and a broad nasal base with bifid nose, but can also be a carrier of the mutation yet stay clinically unaffected.
- This can be an ethnic index or an indication for hypertelorism or hypotelorism, if it is combined with abnormal relation to the interpupillary distance ( A D STEAS ).
- Using an ultrasound, Pallister-Killian may be diagnosed through observation of hypertelorism, broad neck, shorts limbs, abnormal hands or feet, diaphragmatic hernia, and hydramnios.
- A missense mutation in " ACTG1 " at ptosis, excessively-arched eyebrows, hypertelorism, ocular colobomata, lissencephaly, short stature, seizures and hearing loss.
- Other possible symptoms of lissencephaly include telecanthus, estropia, hypertelorism, varying levels of mental retardation, cerebellar hypoplasia, corpus callosum aplasia, and decreased muscle tone and tendon reflexes.
- Common physical malformations are : craniosynostosis of the coronal suture ( s ), orbital hypertelorism, frizzy curled hair, longitudinal ridging and / or splitting of the nails, and facial asymmetry.
- Dr . Noonan produced a paper entitled " Hypertelorism with Turner Phenotype " in 1968, and in 1971 at the Symposium of Cardiovascular defects, the name'Noonan syndrome'became officially recognized.
- Exophthalmos ( bulging eyes due to shallow eye sockets after early fusion of surrounding bones ), hypertelorism ( greater than normal distance between the eyes ), and psittichorhina ( beak-like nose ) are also symptoms.
- In a broader sense, " triangular face " encompasses a constellation of a hypoplastic face with prominent zygomatic arches, orbital hypertelorism, sunken cheeks, down-turned mouth, and occasionally brownish facial discolouration.
- Those suffering of this syndrome often exhibit specific facial features such as a broad forehead, arched eyebrows, ptosis ( droopy eyelids ), hypertelorism ( widely spaced eyes ), low-set ears and a triangle shaped mouth.
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