- A
genetic disorder is a
health problem caused by one or more
abnormalities in the genome. It can be
caused by a
mutation in a
single gene (monogenic) or...
-
Heredofamilial amyloidosis is an
inherited condition that may be
characterized by
systemic or
localized deposition of
amyloid in body tissues.: 522 Amyloidosis...
-
Amyloidosis is a
group of
diseases in
which abnormal proteins,
known as
amyloid fibrils,
build up in tissue.
There are
several non-specific and
vague signs...
-
amyloid neuropathies (or
familial amyloidotic neuropathies,
neuropathic heredofamilial amyloidosis,
familial amyloid polyneuropathy) are a rare
group of autosomal...
- PMID 11746622. S2CID 9540572.
Critchley M (1949). "Observations on
essential (
heredofamilial) tremor". Brain. 72 (2): 113–139. doi:10.1093/brain/72.2.113. PMID 18136705...
-
porphyria Hereditary coproporphyria Hereditary gelsolin amyloidosis Heredofamilial amyloidosis Hunter syndrome Hurler syndrome (gargoylism, mucopolysaccharidosis...
- Scandinavica. Supplementum. 265:1-124. Kugelberg, E., Welander, L. (1956). "
Heredofamilial juvenile muscular atrophy simulating muscular dystrophy".
Archives of...
-
Siegfried Joseph Thannhauser):
Muscular shortening and dystrophy. A
heredofamilial disease. In:
Archives of
Neurology and
Psychiatry 1941; Vol. 46: 654–664...
-
people from four
families who
suffered from an "autosomal dominant,
heredofamilial myopathy"
which consisted in "slowly
progressive ptosis and extraocular...
-
pathophysiology of
familial pseudopelade of
Brocq may be
influenced by
heredofamilial variables,
according to a
small number of case
reports and case series...
