Literature DB >> 27618595

Allgrove syndrome with prominent neurological symptoms. Case Report.

Martin Jerie1, Zdenek Vojtech1, Hana Malikova2, Sylva Prochazkova3, Zuzana Vackova4, Arndt Rolfs5.   

Abstract

We report a young woman with the clinical picture of Allgrove syndrome in whom neurological symptoms are prominent. It usually presents in the first decade of life with a deficiency of tears, recurrent vomiting and dysphagia due to achalasia, severe hypoglycemic seizures and shock due to adrenal insufficiency. Neurological symptoms such as hyperreflexia, dysarthria, hypernasal speech, ataxia, sensory impairment, muscle weakness, and mental retardation are extremely slow to develop and manifest at a later age. Diagnosis was based on clinical presentation and laboratory findings. She is the first patient from the Czech Republic with genetic confirmation of Allgrove syndrome. This patient is one of about 100 cases described in the literature and one of the few patients with all the main typical clinical features.

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Year:  2016        PMID: 27618595

Source DB:  PubMed          Journal:  Neuro Endocrinol Lett        ISSN: 0172-780X            Impact factor:   0.765


  2 in total

1.  A Novel Variant in Triple A Syndrome.

Authors:  E Demet Akbaş; Ö Özalp Yüreğir; Ö Anlaş; Z Özçelik; O Zerrin Tolunay
Journal:  Acta Endocrinol (Buchar)       Date:  2021 Jul-Sep       Impact factor: 0.877

2.  Triple A syndrome (Allgrove syndrome): improving outcomes with a multidisciplinary approach.

Authors:  Myrto Eleni Flokas; Michael Tomani; Levon Agdere; Brande Brown
Journal:  Pediatric Health Med Ther       Date:  2019-08-29
  2 in total

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