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Wolcott-Rallison syndrome: a case with endocrine and exocrine pancreatic deficiency and pancreatic hypotrophy |
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| Authors: | Pierre Castelnau Martine Le Merrer Catherine Diatloff-Zito Eve Marquis Marie-Joseph Tête Jean-Jacques Robert |
| Affiliation: | Fédération de Pédiatrie, Diabète de l'Enfant et de l'Adolescent, H?pital Necker - Enfants Malades, 149, rue de Sèvres, 75743 Paris Cedex 15, France Tel.: +33-1-44494833, Fax: +33-1-44381536, FR Service de Génétique Clinique, INSERM U393, Handicaps Génétiques de l'Enfant, H?pital Necker - Enfants Malades, Paris, France, FR INSERM U383, Génétique, Chromosome et Cancer, H?pital Necker - Enfants Malades, Université Paris V, Paris, France, FR Croix-Rouge, Centre Thérapeutique Pédiatrique Margency, France, FR |
| Abstract: | Clinical analysis and genetic investigations of new cases of Wolcott-Rallison syndrome are needed to evaluate the role of the gene(s) directly or indirectly implicated in pancreas development and in the aetiology of the syndrome. |
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