Misdiagnosis of Hidden Causes of Congenital heart defects

Underlying conditions list:

The list of possible underlying conditions mentioned in various sources for Congenital heart defects includes:

• Maternal infection during pregnancy:
  • Gestational diabetes
  • SLE
  • Rubella
  • Certain drugs during pregnancy
• Spondyloepimetaphyseal dysplasia with joint laxity - congenital heart disease
• Short limbs - abnormal face - congenital heart disease - congenital heart disease
• Sakati syndrome - congenital heart disease
• Zunich neuroectodermal syndrome - Congenital heart disease
• Loeys-Dietz syndrome - congenital heart disease
• Humerospinal dysostosis - congenital heart disease - congenital heart disease
• Chromosome 8, monosomy 8p23.1 - congenital heart disease
• Patent ductus arteriosus
• Down syndrome - congenital heart disease
• Forney Robinson Pascoe syndrome - congenital heart disease
• Chromosome 1, trisomy 1q32 qter - congenital cardiac anomaly
• Blepharophimosis syndrome Ohdo type - congenital heart disease
• Axial mesodermal dysplasia spectrum - congenital heart disease
• Lymphoedema-distichiasis syndrome
• CHARGE Syndrome - congenital heart disease
• Acrocephalopolydactyly II - congenital heart disease
• Atrial septal defect (ostium secundum)
• Ventricular septal defect
• Lissencephaly syndrome type 1 - congenital heart disease
• Cardiocranial syndrome - congenital heart disease
• Ho Kaufman-Mcalister syndrome - congenital heart disease
• Congenital heart disease, ptosis, hypodontia, craniosynostosis - congenital heart disease
• Gay-Feinmesser-Cohen syndrome - congenital heart disease
• Fallot's tetralogy
• Trisomy 21 mosaicism - congenital heart disease
• Trisomy 12 mosaicism - congenital heart disease
• Single upper central incisor - congenital heart disease
• Hurst-Hallam-Hockey syndrome - congenital heart disease
• Chromosome 13 trisomy syndrome - congenital heart disease
• Yorifuji Okuno syndrome - Congenital heart disease
• Trisomy 13 mosaicism - congenital heart disease
• Maternal hyperphenylalaninemia - congenital heart disease
• DiGeorge's syndrome - congenital heart disease
• Congenital heart disease radio ulnar synostos mental retardation - congenital heart disease
• Transposition of great arteries
• VACTERL association - congenital heart disease
• Chromosome 19q, partial duplication - congenital heart disease
• Williams syndrome
• Coarctation of aorta
• Pfeiffer syndrome Type 3 - congenital heart disease
• Lissencephaly - congenital heart disease
• Goossens-Devriendt syndrome - congenital heart disease
• Edwards Syndrome - Congenital heart disease
• Chromosome 7 ring syndrome - congenital heart disease
• Blepharoptosis - aortic anomaly - congenital heart disease
• Eisenmenger's syndrome
• Atrial septal defect (ostium primum)

Congenital heart defects as a complication:

Other conditions that might have Congenital heart defects as a complication might be potential underlying conditions. The list of conditions listing Congenital heart defects as a complication includes:

• CHARGE Syndrome
• Childbirth
• Down Syndrome

Congenital heart defects as a symptom:

Conditions listing Congenital heart defects as a symptom may also be potential underlying conditions.

You may also want to research other symptoms in our Symptoms Center.

• 14q+ syndrome
• 22q11.2 deletion syndrome
• 7p2 Monosomy Syndrome
• ACPS III
• Acrocephalopolydactyly - Cardiac Disease - Ear, Skin and Lower Limb Defects
• Acrocephalopolydactyly II
• Acrocephalopolysyndactyly type III
• Al Gazali Aziz Salem syndrome
• Arterial occlusive disease, progressive - hypertension - heart defects - bone fragility - brachysyndactyly
• Axial mesodermal dysplasia spectrum
• Barrow-Fitzsimmons Syndrome
• Blepharophimosis syndrome Ohdo type
• Blepharoptosis - aortic anomaly
• Brain malformation - congenital heart disease - postaxial polydactyly
• Cardiocranial syndrome
• Cervical ribs, sprengel anomaly, anal atresia, urethral obstruction
• Chromosome 1, uniparental disomy 1q12 q21
• Chromosome 10p deletion syndrome
• Chromosome 11q duplication syndrome
• Chromosome 12 trisomy
• Chromosome 12, Isochromosome 12p Mosaic
• Chromosome 12p tetrasomy syndrome
• Chromosome 13 trisomy syndrome
• Chromosome 15 Ring
• Chromosome 15q duplication syndrome
• Chromosome 15q, trisomy
• Chromosome 17p, partial duplication
• Chromosome 19q, partial duplication
• Chromosome 1p deletion syndrome
• Chromosome 2, trisomy 2p
• Chromosome 22q deletion
• Chromosome 22q11.2 deletion syndrome
• Chromosome 2p duplication syndrome
• Chromosome 3, trisomy 3p
• Chromosome 5, trisomy 5q
• Chromosome 5q duplication syndrome
• Chromosome 6, trisomy 6p
• Chromosome 7 ring syndrome
• Chromosome 7, Monosomy 7p2
• Chromosome 7, terminal 7p deletion
• Chromosome 8 deletion
• Chromosome 8, monosomy 8p23.1
• Chromosome 8, mosaic trisomy
• Chromosome 8, trisomy 8q
• Chromosome 8p duplication syndrome
• Chromosome 8q duplication syndrome
• Chromosome 9, partial trisomy 9p
• Chromosome 9, Trisomy 9p (Multiple Variants)
• Chromosome 9/mosaic
• Collins-Dennis-Clarke-Pope Syndrome
• Complete Trisomy 18 syndrome
• Congenital heart disease radio ulnar synostos mental retardation
• Congenital heart disease, ptosis, hypodontia, craniosynostosis
• Conotruncal heart malformations
• Craniosynostosis - congenital heart disease - mental retardation
• Del(1) (q25-q32)
• Deletion 11q
• Deletions of chromosome 8
• DiGeorge's syndrome
• Distichiasis with Congenital Anomalies of the heart and Peripheral Vasculature
• Dup(1) (q25-q32)
• Duplication 18
• Duplication 2p
• Duplication 5q
• Duplication 6p
• Duplication 8q
• Duplication 9p partial
• Edward Syndrome
• Edwards Syndrome
• Emanuel syndrome
• Forney Robinson Pascoe syndrome
• Franceschini-Vardeu-Guala syndrome
• Gay-Feinmesser-Cohen syndrome
• Genée-Wiedemann syndrome
• Goossens-Devriendt syndrome
• Ho Kaufman-Mcalister syndrome
• Holt-Oram Syndrome
• Humerospinal dysostosis - congenital heart disease
• Hunter-Mcdonald syndrome
• Hurst-Hallam-Hockey syndrome
• Insulin Dependent Diabetes Mellitus - Teratogenic Agent
• Jacobsen syndrome
• Larsen syndrome, recessive type
• Laryngeal web congenital heart disease short stature
• Lissencephaly
• Lissencephaly syndrome type 1
• Loeys-Dietz syndrome
• Maternal hyperphenylalaninemia
• Microcephaly - microphthalmia - ectrodactyly of lower limbs - prognathism
• Microphthalmia syndromic, type 8
• Multiple Skeletal abnormalities with Anterior Segment Anomalies of the Eye and Early Lethality
• Neurofaciodigitorenal syndrome
• Pallister Killian Mosaic Syndrome
• Pallister Mosaic Syndrome Tetrasomy 12p
• Pallister-Hall Syndrome
• Partial Trisomy 18 Syndrome
• Pfeiffer syndrome Type 3
• Phenylketonuria - Teratogenic Agent
• Powell-Chandra-Saal syndrome
• Sakati syndrome
• Short limbs - abnormal face - congenital heart disease
• Short stature webbed neck heart disease
• Single upper central incisor
• Spondyloepimetaphyseal dysplasia with joint laxity
• Tabatznik syndrome
• Tracheal stenosis syndrome
• Trisomy 12 mosaicism
• Trisomy 13 mosaicism
• Trisomy 18 mosaicism
• Trisomy 18 Syndrome
• Trisomy 21 mosaicism
• Trisomy 8 mosaicism
• VACTERL association
• VACTERL hydrocephaly
• VACTERL with hydrocephalus, X-linked
• Van der Woude syndrome
• Van der Woude syndrome 2
• Yorifuji Okuno syndrome
• Zunich neuroectodermal syndrome
• Zunich-Kaye syndrome

About underlying conditions:

With a diagnosis of Congenital heart defects, it is important to consider whether there is an underlying condition causing Congenital heart defects. These are other medical conditions that may possibly cause Congenital heart defects. For general information on this form of misdiagnosis, see Underlying Condition Misdiagnosis or Overview of Misdiagnosis.
 » Next page: Treatments for Congenital heart defects

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• Doctors and Medical Specialists for Congenital heart defects
• Cure Research for Congenital heart defects
• Deaths from Congenital heart defects
• Statistics about Congenital heart defects

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