Literature DB >> 15990695

Wolfram syndrome. How much could knowledge challenge the fate? A case report.

Lea Paola Fabbri1, Maria Nucera, Antonello Grippo, Adriana Menicucci, Maria Laura De Feo, Chiara Becchi, Mohamed Al Malyan.   

Abstract

BACKGROUND: Wolfram syndrome (WS) is a rare, autosomic recessive genetic disorder. The mortality rate of WS is about 65% before 35 years of age. It presents diagnostic challenges in the clinical practice due to its incomplete characterization. This report represents the first case of undiagnosed Wolfram syndrome in a patient over 53 years old. CASE REPORT: A 53-year-old white woman developed a respiratory complication necessitating extended ICU care and respiratory rehabilitation. This respiratory complication proved to be a consequence of undiagnosed WS.
CONCLUSIONS: The report discusses the clinical elements that suggested the diagnosis, the problems related to the ICU management of this patient, in particular the weaning difficulties, and the need for rehabilitation. Finally, the report considers the ethical aspect of timely diagnosis on the course and outcome of WS.

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Mesh:

Year:  2005        PMID: 15990695

Source DB:  PubMed          Journal:  Med Sci Monit        ISSN: 1234-1010


  2 in total

1.  The Expression of RAAS Key Receptors, Agtr2 and Bdkrb1, Is Downregulated at an Early Stage in a Rat Model of Wolfram Syndrome.

Authors:  Marite Punapart; Kadri Seppa; Toomas Jagomäe; Mailis Liiv; Riin Reimets; Silvia Kirillov; Allen Kaasik; Lieve Moons; Lies De Groef; Anton Terasmaa; Eero Vasar; Mario Plaas
Journal:  Genes (Basel)       Date:  2021-10-28       Impact factor: 4.096

2.  Wolfram syndrome (diabetes insipidus, diabetes, optic atrophy, and deafness): clinical and genetic study.

Authors:  Giuseppe d'Annunzio; Nicola Minuto; Elena D'Amato; Teresa de Toni; Fortunato Lombardo; Lorenzo Pasquali; Renata Lorini
Journal:  Diabetes Care       Date:  2008-06-19       Impact factor: 19.112

  2 in total

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