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What (who) is systemic amyloidosis - definition

HEREDITARY AMYLOIDOSIS

Familial amyloidotic polyneuropathy; Systemic senile amyloidosis; Familial Amyloid Polyneuropathy; TTR Amyloidosis; Senile Cardiac TTR-Amyloidosis; Corino de Andrade's disease; Transthyretin amyloidosis; Portuguese type amyloidosis; Transthyretin-related hereditary amyloidosis; Hereditary transthyretin-mediated amyloidosis

AL amyloidosis

MEDICAL CONDITION

Amyloid light chain; Primary amyloidosis; Primary systemic amyloidosis; Systemic AL amyloidosis; AL amyloid; Primary Systemic Amyloidosis; AL Amyloidosis

Amyloid light-chain (AL) amyloidosis, also known as primary amyloidosis, is the most common form of systemic amyloidosis in the US. The disease is caused when a person's antibody-producing cells do not function properly and produce abnormal protein fibers made of components of antibodies called light chains.

https://en.wikipedia.org/wiki/AL_amyloidosis

Familial amyloid polyneuropathy

Familial amyloid polyneuropathy, also called transthyretin-related hereditary amyloidosis, transthyretin amyloidosis abbreviated also as ATTR (hereditary form), or Corino de Andrade's disease, is an autosomal dominant neurodegenerative disease. It is a form of amyloidosis, and was first identified and described by Portuguese neurologist Mário Corino da Costa Andrade, in 1952.

https://en.wikipedia.org/wiki/Familial_amyloid_polyneuropathy

LECT2 amyloidosis

HUMAN DISEASE

Lect2 amyloidosis

LECT2 Amyloidosis (ALECT2) is a form of amyloidosis caused by the LECT2 protein. It was found to be the third most common (~3% of total) cause of amyloidosis in a set of more than 4,000 individuals studied at the Mayo Clinic; the first and second most common forms the disorder were AL amyloidosis and AA amyloidosis, respectively.

https://en.wikipedia.org/wiki/LECT2_amyloidosis

Wikipedia

Familial amyloid polyneuropathy

Familial amyloid polyneuropathy, also called transthyretin-related hereditary amyloidosis, transthyretin amyloidosis abbreviated also as ATTR (hereditary form), or Corino de Andrade's disease, is an autosomal dominant neurodegenerative disease. It is a form of amyloidosis, and was first identified and described by Portuguese neurologist Mário Corino da Costa Andrade, in 1952. FAP is distinct from senile systemic amyloidosis (SSA), which is not inherited, and which was determined to be the primary cause of death for 70% of supercentenarians who have been autopsied. FAP can be ameliorated by liver transplantation.

https://en.wikipedia.org/wiki/Familial amyloid polyneuropathy