Pallister-Killian mosaic syndrome is a developmental disorder that affects many parts of the body. This condition is characterized by extremely weak muscle ...
Important It is possible that the main title of the report Pallister Killian Mosaic Syndrome is not the name you expected. Please check the synonyms ...
Pallister–Killian syndrome (also tetrasomy 12p mosaicism or Pallister mosaic aneuploidy syndrome) is an extremely rare genetic disorder occurring in humans.
Pallister-Killian mosaic syndrome is a disorder that is characterized by extremely weak muscle tone (hypotonia) in infancy and early childhood ...
Symptoms of the following disorders can be similar to those of Pallister- Killian Mosaic Syndrome. Comparisons may be useful for a differential diagnosis:
Pallister Killian Mosaic Syndrome information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis.
Pallister-Killian Mosaic Syndrome is a rare chromosomal disorder caused by the presence of four copies of the short arm of chromosome 12 instead of the normal two.
General Discussion. Pallister-Killian Mosaic Syndrome is a rare chromosomal disorder caused by the presence of four copies of the short arm of chromosome ...
COMPASSIONATE ALLOWANCE INFORMATION. PALLISTER-KILLIAN SYNDROME . ALTERNATE NAMES . Pallister Mosaic Syndrome; Pallister-Killian Mosaic Syndrome; Killian Syndrome ...
Pallister-Killian syndrome (PKS) is a rare, sporadic, polydysmorphic condition that often has highly distinctive features. The clinical features are highly ...