Doctor insights on:
Pallister Killian Syndrome Prognosis
No: Pallister killien is a random defect of the 12th chromosome. It has muliple far reaching effects. It is evidenced by hypotonia, developmental delay, itellectual impairment, coarse features, sparse hair. It is not hereditary. Once a person has it one can only cope with the defect to try to ameliorate the symptoms, ie hearing defects with a hearing aid, etc. ...Read moreSee 1 more doctor answer
See a doctor: I think you mean foster kennedy syndrome in which an enlarging brain tumor obstructs one optic nerve causing atrophy to that nerve, and also causes elevation of the pressure in the brain causing optic nerve edema (papilledema) in the other nerve. This is a rare circumstance which requires immediate attention by a neuro-ophthalmologist or neurosurgeon. ...Read more
Medically and surgic: It is a chromosomal disorder which results from an extra anomalous chromosome. Sometimes it can be detected prenatally by ultrasound. There are specific and varied physical features that identify the syndrome. ...Read more
Turner's Syndrome: The prognosis for turner's syndrome diagnosed at birth is usually good. They will be short. They have streaked gonads. They can have a webbed neck. There can be lymphedema. There can be associated perceptual problems. They are not necessarily mentally retarded. There can be coarctation of the aorta. ...Read moreSee 1 more doctor answer
Crouzon: Crouzon craniofacial dysostosis was described by crouzon in 1912. The genetic cause was not identified until 1994 and the credit goes to a number of different geneticists - reardon and preston independently helped narrow the genetic inheritance to the fgfr2 gene. ...Read more
Crouzonodermoskeleta: Crouzonodermoskeletal syndrome involves premature joining skull bones & acanthosis nigricans. Louis edouard octave crouzon (1874–1938) published “une nouvelle famille atteinte de dysostose cranio-faciale héréditaire” in archives de médecine DES enfants, paris, in 1915. So I am guessing that he discovered crouzon syndrome prior to that publication. ...Read more
Ramsay Hunt Type II: is caused by reactivation of the Varicella or Chickenpox virus in the geniculate ganglion, a collection of of nerve cells & fibers of the Facial Nerve. Prognosis depends on age, competence of immune system, extent & severity of impairments from Facial Nerve damage. Milder cases treated with antiviral medication & steroids within 3 days of symptom onset have a 70-75% chance of recovery. ...Read more
Yes: The cure for hellp syndrome is delivery. The good news is it usually develops late in the pregnancy. Although the baby maybe premature, many of them will do fine. Your doctor may give steroids in order to help the baby's lungs mature more quickly. Medication maybe used to control blood pressure, prevent seizures, and correct problems with blood clotting. Transfusion of blood poducts maybe needed. ...Read more
Inherited Condition: 1 / 20, 000- 60, 000 newborns are born w/ this condition which can cause malformations of heart, lungs, kidneys, gut & genitalia. Affected babies often have small head size, fused second & third toes &sometimes extra fingers and toes. There can be learning and behavior problems from mild to approaching autism in severity. Infants may grow more slowly, have weaker muscle tone, & have feeding issues. ...Read more
Genetic evaluation: A clinical geneticist observed a person with Crouzon disease, and noticed acanthuses nigricans with no diabetes. Published the association. Then a second case report. finally enough for the splitters to win, and they made up the godawful name, which seems to be attracting a lot of questions suddenly, and I really would like to know if this is cause some biology professor handing out homework. ...Read more
What do they have in: They all have abnormalities of autonomics and other nervous sytem problems. ...Read more
Depends: On the course of the disease, organ involvement, baseline health status, the aggressiveness of the condition, and many other factors (response to treatment, etc.). ...Read more
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