ACROGERIA

 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1952-2017
01219522016

Papers overview

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2003
2003
Acrogeria is one of the premature aging syndromes with an unknown mode of inheritance. Familial cases are quite rare. A report of… (More)
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1996
1996
We have recently analysed by histological, protein and molecular DNA techniques 23 mutations of the collagen III gene (COL3A1… (More)
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1987
1987
We report the skeletal abnormalities in a 4 1/2-year-old boy with acrogeria, a progeroid syndrome of premature aging of the skin… (More)
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1987
1987
An 11-year-old patient with clinically typical acrogeria is presented. She had wrinkled 'old-appearing' acral skin, thin skin on… (More)
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1986
1986
A familial case of acrogeria, occurring in a mother and her daughter, is reported. A 12-year old mentally retarded girl was seen… (More)
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1985
1985
We report on a 17-year-old patient suffering from generalized mottled hyperpigmentation and multiple telangiectatic lesions of… (More)
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1984
1984
A case of acrogeria, a premature aging syndrome with acral distribution, is reported in association with perforating elastoma and… (More)
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1980
1980
A mother and her oldest son suffering from acrogeria are described; in the mother the disease was complicated by elastosis… (More)
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1980
1980
Evidence is presented that type IV of the Ehlers-Danlos syndrome (EDS IV) is genetically variable. A benign autosomal dominant… (More)
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1977
1977
A case of acrogeria in a 12-year-old girl is reported. Acrogeria is a rare, nonhereditary, probably congenital disease of which… (More)
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