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cornelia de lange syndrome: a case report with a novel congenital heart disease association
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نویسنده
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allugmani mohammad d. ,el-harbi mazen k. ,khoshhal mohammad s. ,alrabghy najia ,almutery sabreen ,alawfi abdulsalam d. ,abo-haded hany m.
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منبع
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journal of comprehensive pediatrics - 2022 - دوره : 13 - شماره : 4 - صفحه:1 -5
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چکیده
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Introduction: cornelia de lange syndrome (cdls) is a rare non-hereditary syndrome. the key diagnosis is unique facial features, limb anomalies, and growth retardation. cardiac defects with gastrointestinal and genitourinary anomalies may be associated. case presentation: this is a case of neonatal cdls that we think is interesting due to its association with a novel congenital heart complex. conclusions: patients with cdls have a high incidence of congenital heart disease (chd), so a cardiologic study of all of these patients is suggested.
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کلیدواژه
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cornelia de lange syndrome ,craniofacial ,congenital heart defects ,multidisciplinary approach
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آدرس
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maternity and children hospital (mch), pediatric cardiology unit, department of pediatrics, saudi arabia, taibah university, faculty of medicine, saudi arabia, taibah university, faculty of medicine, saudi arabia, maternity and children hospital (mch), pediatric cardiology unit, department of pediatrics, saudi arabia, maternity and children hospital (mch), pediatric cardiology unit, department of pediatrics, saudi arabia, taibah university, faculty of medicine, department of pediatrics, saudi arabia, taibah university, faculty of medicine, department of pediatrics, saudi arabia##egypt. mansoura university, faculty of medicine, department of pediatrics, egypt
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پست الکترونیکی
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hany_haded@yahoo.com
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Authors
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