A new type of Ehlers-Danlos syndrome associated with tortuous systemic arteries in a large kindred from Qatar

Aim: To describe the clinical spectrum of anomalies of a new type of Ehlers‐Danlos syndrome in 32 patients from a large inter‐related extended family in Qatar. Methods: Among the 32 patients (from 22 families), there were 6 affected pairs of siblings and 2 families with 3 affected siblings. The male...

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Veröffentlicht in:	Acta Paediatrica 2003-04, Vol.92 (4), p.456-462
Hauptverfasser:	Wahab, A Abdul, Janahi, IA, Eltohami, A, Zeid, A, Haque, NF Ul, Teebi, AS
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Bifid pulmonary artery Biological and medical sciences Carbohydrates (enzymatic deficiencies). Glycogenosis Child Child, Preschool DNA markers Ehlers-Danlos syndrome Ehlers-Danlos Syndrome - complications Ehlers-Danlos Syndrome - diagnosis Ehlers-Danlos Syndrome - genetics elongated aortic arch Errors of metabolism Family Female Humans Infant Infant, Newborn Male Medical sciences Metabolic diseases Outcome Assessment (Health Care) peculiar facial features Qatar Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis Severity of Illness Index Torsion Abnormality - complications Torsion Abnormality - diagnosis Torsion Abnormality - genetics Tropical medicine Vascular Diseases - complications Vascular Diseases - diagnosis Vascular Diseases - genetics
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