Literature DB >> 327549

Biochemical identification of homogentisic acid pigment in an ochronotic egyptian mummy.

F F Stenn, J W Milgram, S L Lee, R J Weigand, A Veis.   

Abstract

Roentgenograms of an Egyptian mummy, dating from 1500 B.C., showed extensive calcification of the intervertebral discs and articular narrowing in both hip and knee joints. Biopsy cores from the right hip showed parallel black zones in the region of the articular surfaces, leading to a clinical diagnosis of ochrinosis. The black pigment was extracted, analyzed, and compared to an air-oxidized homogentistic acid polymer. The two substances apparently were identical. The chemical evidence thus confirms the clinical finding of ochronosis, an autosomal recessive disorder. This is, so far as known, the earliest verified case of this disorder.

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Year:  1977        PMID: 327549     DOI: 10.1126/science.327549

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  14 in total

1.  Identification of forty cases with alkaptonuria in one village in Jordan.

Authors:  Mohammed Al-Sbou; Nesrin Mwafi; Mohammad Abu Lubad
Journal:  Rheumatol Int       Date:  2011-11-16       Impact factor: 2.631

2.  Ochronotic involvement of the aortic and mitral valves in a 72-year-old man.

Authors:  Atakan Atalay; Ugur Gocen; Yuksel Basturk; Erkan Kozanoglu; Hafize Yaliniz
Journal:  Tex Heart Inst J       Date:  2015-02-01

3.  Nine cases of Alkaptonuria in one family in southern Jordan.

Authors:  Mohammed Al-Sbou; Nesrin Mwafi
Journal:  Rheumatol Int       Date:  2010-12-03       Impact factor: 2.631

4.  Hope: a panacea unrecognized.

Authors:  A O Obayuwana
Journal:  J Natl Med Assoc       Date:  1980-01       Impact factor: 1.798

Review 5.  Alkaptonuric ochronosis with aortic valve and joint replacements and femoral fracture: a case report and literature review.

Authors:  Alexander A Fisher; Michael W Davis
Journal:  Clin Med Res       Date:  2004-11

6.  Novel mutations in the homogentisate 1,2 dioxygenase gene identified in Jordanian patients with alkaptonuria.

Authors:  Mohammed Al-sbou
Journal:  Rheumatol Int       Date:  2011-03-25       Impact factor: 2.631

Review 7.  Garrod's Croonian Lectures (1908) and the charter 'Inborn Errors of Metabolism': albinism, alkaptonuria, cystinuria, and pentosuria at age 100 in 2008.

Authors:  Charles R Scriver
Journal:  J Inherit Metab Dis       Date:  2008-10-12       Impact factor: 4.982

8.  Ochronosis: a case report with severe ochronotic arthropathy.

Authors:  A Peretz; M Dupont; J P Famaey
Journal:  Clin Rheumatol       Date:  1983-09       Impact factor: 2.980

9.  Mutation spectrum of homogentisic acid oxidase (HGD) in alkaptonuria.

Authors:  Thierry Vilboux; Michael Kayser; Wendy Introne; Pim Suwannarat; Isa Bernardini; Roxanne Fischer; Kevin O'Brien; Robert Kleta; Marjan Huizing; William A Gahl
Journal:  Hum Mutat       Date:  2009-12       Impact factor: 4.878

Review 10.  Alkaptonuria.

Authors:  Jemma B Mistry; Marwan Bukhari; Adam M Taylor
Journal:  Rare Dis       Date:  2013-12-18
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