Dura mater involvement in ochronosis (alkaptonuria)

Archives of Pathology and Laboratory Medicine

Volumn 125, Issue 7, 2001, Pages 961-963

  Liu, W ^a   Prayson, R A ^a  

^a LERNER RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PIGMENT;

AGED; ALKAPTONURIA; ARTICLE; AUTOPSY; CASE REPORT; CONNECTIVE TISSUE; DURA MATER; FEMALE; HEART; HUMAN; HUMAN TISSUE; JOINT; KIDNEY; OCHRONOSIS; PIGMENTATION; SKIN;

AGED; ALKAPTONURIA; BRAIN; DURA MATER; FATAL OUTCOME; FEMALE; HUMANS; OCHRONOSIS;

EID: 0034936594     PISSN: 00039985     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (10)

1. Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2
2. Nevomelanocytic proliferations in the central nervous system of children
3. Alcaptonuria, ochronosis, arthritis and ruptured intervertebral disc complicated by homologous serum reaction
4. Cutaneous deposition diseases, part II
5. In vivo inhibition of chick embryo lysyl hydroxylase by homogentisic acid: A proposed connective defect in alkaptonuria
6. Studies on ochronosis: A report of a case with death from ochronotic nephrosis
7. Cardiovascular ochronosis
8. Alkaptonuria and renal failure: A case report and review of the literature
9. Discoloration of the teeth in alkaptonuria (ochronosis) and parkinsonism
10. Long-term followup of a new case of hawkinsinuria