Hereditary hyperferritinemia cataract syndrome;Das hereditäre Hyperferritinämie-Katarakt-Syndrom

Deutsche Medizinische Wochenschrift

Volumn 136, Issue 38, 2011, Pages 1895-1898

  Holzgreve, H ^a  

^a Internist Kardiologische Praxis   (Germany)

Author keywords

autosomal dominant trait; cataract; hyperferritinemia

Indexed keywords

FERRITIN; TRANSFERRIN; IRON; IRON REGULATORY FACTOR;

ADULT; ANAMNESIS; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; CATARACT; CATARACT EXTRACTION; DIAGNOSTIC ACCURACY; DIFFERENTIAL DIAGNOSIS; FERRITIN BLOOD LEVEL; GENE MUTATION; GENETIC DISORDER; HEREDITARY HYPERFERRITINEMIA CATARACT SYNDROME; HETEROZYGOSITY; HUMAN; HYPERFERRITINEMIA; INTERNATIONAL NORMALIZED RATIO; LABORATORY TEST; MALE; SYNDROME; TREATMENT INDICATION; BLOOD; CHROMOSOME ABERRATION; CONGENITAL MALFORMATION; DOMINANT GENE; GENETIC SCREENING; GENETICS; HETEROZYGOTE DETECTION; HYPERTENSION, RENAL; INFERIOR CAVA VEIN; IRON METABOLISM DISORDERS; KIDNEY; METABOLISM; NUCLEOTIDE SEQUENCE; PHENOTYPE; POSTTHROMBOTIC SYNDROME; VENOUS THROMBOSIS;

ADULT; CATARACT; CATARACT EXTRACTION; CHROMOSOME ABERRATIONS; DNA MUTATIONAL ANALYSIS; FERRITINS; GENES, DOMINANT; GENETIC TESTING; HETEROZYGOTE DETECTION; HUMANS; HYPERTENSION, RENAL; IRON; IRON METABOLISM DISORDERS; IRON-REGULATORY PROTEINS; KIDNEY; MALE; PHENOTYPE; POSTTHROMBOTIC SYNDROME; TRANSFERRIN; VENA CAVA, INFERIOR; VENOUS THROMBOSIS;

EID: 80052856750     PISSN: 00120472     EISSN: 14394413     Source Type: Journal    
DOI: 10.1055/s-0031-1286359     Document Type: Article

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