Gallawardena Syndrome

Gallavardens syndrome Gallavardens syndrome is a rare genetic disease that manifests itself in the form of kidney and cardiovascular dysfunction. It was discovered by the French cardiologist Louis Gallawardenis at the beginning of the 20th century.

The disease is characterized by impaired renal function, which

Gallavard-Fanconi syndrome (GFS): This is a rare genetic abnormality caused by a mutation in the fetoprotein gene on the X chromosome. It results in multiple abnormalities: mental retardation, microcephaly, a large head and face, a torso with abnormally thin skin, hands and feet, several missing teeth, and digestive problems.

HPS is often associated with other genetic syndromes such as Williams syndrome, Sturge-Weber syndrome, Fanconi syndrome, and Didriksonan syndrome. It can also be caused by chromosomal abnormalities or exposure to medications. Symptoms of HPS may appear from birth or later in life and often worsen with age. Cognitive problems, including

Gallawardeni syndrome is a rare hereditary disease that occurs due to problems with the functioning of the heart and lungs. It occurs in people over 65 years of age and usually causes death within months or years. However, in some cases, the condition may not be as serious and patients may live much longer.

Gallawardeni disease was first described by French cardiologist Ludovic Gallat