Literature DB >> 11876140

[DiGeorge syndrome. An underdiagnosed disease category with different clinical features].

A Graesdal1, P Surén, S Vadstrup.   

Abstract

BACKGROUND: DiGeorge syndrome is estimated to affect one in every 3,000-4,000 live-born individuals. The syndrome is also known as velocardiofacial syndrome (VCFS) and conotruncal anomaly face syndrome (CTFS). The most common clinical features are mental retardation, congenital heart anomalies, primary hypoparathyroidism (with hypocalcaemia), aplasia or hypoplasia of the thymus, and a dysmorphic face. 90% of the affected individuals have a deletion at the long arm of chromosome 22. 80-90% of those deletions are de novo mutations.
MATERIAL AND METHODS: This article presents the case of a 32-year-old woman who was diagnosed with DiGeorge syndrome after a grand mal seizure due to hypocalcaemia. The hypocalcaemia was caused by primary hypoparathyroidism. We also give a brief review of the current state of knowledge about DiGeorge syndrome. RESULTS AND
INTERPRETATION: DiGeorge syndrome is probably underdiagnosed. A correct and early diagnosis is important in order to prevent medical complications, e.g. hypocalcaemia and hypothyrosis, and to evaluate the patient's overall need of care.

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Year:  2001        PMID: 11876140

Source DB:  PubMed          Journal:  Tidsskr Nor Laegeforen        ISSN: 0029-2001


  1 in total

1.  Afebrile Seizures as Initial Symptom of Hypocalcemia Secondary to Hypoparathyroidism.

Authors:  Mahmood Dhahir Al-Mendalawi
Journal:  J Neurosci Rural Pract       Date:  2017 Jul-Sep
  1 in total

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