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• See Prune Belly Syndrome

• List of Sites

• List of Sites
• with Cataracts and Kyphoscoliosis
• See Tricooculodermovertebral Syndrome

• Ectopia Lentis
• Isolated
• ECTOPIA LENTIS, ISOLATED

• List of Sites
• with Cardiopathy and Dysmorphism
• See Van den Ende Brunner Syndrome
• with Diaphragmatic Hernia and Corpus Callosum Agenesis
• See Saal Bulas Syndrome
• with Ectodermal Dysplasia (Ectrodactyly, Ectodermal Dysplasia and Cleft Lip or Palate [EEC] Syndrome, without Cleft Lip or Palate)
• Ectrodactyly - ectodermal dysplasia
• ectrodactyly ectrodermal dysplasia
• and Cleft Lip or Palate (Ectrodactyly, Ectodermal Dysplasia and Cleft Lip or Palate [EEC] Syndrome)
• List of Sites
• -Cleft Palate Syndrome
• ectrodactyly cleft palate syndrome
• ECTRODACTYLY-CLEFT PALATE SYNDROME
• -Macular Dystrophy
• Features Listed For ECTRODACTYLY-ECTODERMAL DYSPLASIA-MACULAR DYSTROPHY (EEM)
• -Polydactyly
• ectrodactyly polydactyly
• ECTRODACTYLY-POLYDACTYLY
• with Spina Bifida and Cardiopathy
• See Kasznica Carlson Coppedge Syndrome

• See Wiskot Aldrich Syndrome

• List of Sites

• List of Sites

• Eisenmenger's Complex
• Eisenmenger's complex
• Eisenmenger's complex
• Eisenmenger Complex
• Also see Atrial Septal Defect

• See Osteogenesis Imperfecta

• See Acrocephalopolydactyly

• See Mucopolysaccharidosis, Type I

• List of Sites

• Emery Driefuss Muscular Dystrophy
• Autosomal Dominant/Type II (Hauptmann Thannhausre Muscular Dystrophy; Muscular Dystrophy with Early Contractures and Cardiomyopathy, Autosomal Dominant; Scapuloilioperoneal Atrophy with Cardiopathy)
• EMERY-DREIFUSS MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT; EDMD2

• AMELOGENESIS IMPERFECTA AND NEPHROCALCINOSIS
• Amelogenesis imperfecta nephrocalcinosis
• Amelogenesis imperfecta nephrocalcinosis

• List of Sites

• Fatal Infantile
• with Olivopontocerebellar Hypoplasia
• See Young McKeever Squier Syndrome

• See Ollier's Disease

• Multiple
• Type I
• See Wermer Syndrome

• Multiple
• See Wermer Syndrome

• See Van Buchem Disease
• Worth Type
• See Worth Syndrome

• See Twins, Conjoined, Craniothoracopagus

• See Nevus Sebaceus of Jadassohn

• List of Sites

• See Ichthyosiform Erythroderma, Congenital, Bullous Form

• Related Books
• Courtney has epilepsy...
• EPILESSIE 
• Support Groups
• Benign
• Familial
• Infantile
• Benign familial infantile convulsions
• BENIGN FAMILIAL INFANTILE CONVULSIONS
• Neonatal
Erosen oireyhtymä
• Convulsions/Epilepsy/Seizures benign familial neonatal
• EPILEPSY, BENIGN NEONATAL, 1; EBN1
• SEIZURES, BENIGN FAMILIAL NEONATAL
• Centralopathic/Centrotemporal (Benign Rolandic Epilepsy, Temporal-Central Focal Epilepsy)
• Centrotemporal epilepsy
• CENTRALOPATHIC EPILEPSY
• with Dementia and Amelogenesis Imperfecta
• See Kohlschutter (Tonz) Syndrome

• See Duncan Disease

• Alport syndrome macrothrombocytopenia
• MACROTHROMBOCYTOPATHY, NEPHRITIS, AND DEAFNESS

• See O'Doherty Syndrome

• DIGITORENOCEREBRAL SYNDROME
• Eronen syndrome
• brachydactyly absence of distal phalanges
• Erosen oireyhtymä 

• See Wagner Syndrome

• See Multiple Pterygium Syndrome

Esophageal Atresia and Tracheoesophageal Fistula

• List of Sites

Euhidrotic Ectodermal Dysplasia

• See Kopysc Barczyk Krol Syndrome

Exencephaly

• EXENCEPHALY : A RARE CASE DIAGNOSED ON ANTENATAL ULTRASOUND (Includes ultrasound)
• Pediatric Pathology (Includes a Photo)
• exencephaly
• Exencephaly – Anencephaly Sequence and its Sonographic Features (Includes ultrasounds)
• Fetus with Exencephaly (Includes drawing)

Exostoses

• Hereditary
• Multiple
• MHE Coalition
• MULTIPLE HEREDITARY EXOSTOSES, and the THE GENETIC CONNECTIONS to CHONDROSARCOMA
• HEREDITARY MULTIPLE EXOSTOSES SUPPORT GROUP
• Multiple Hereditary Exostoes (MHE)
• Osteochondromatosis
• Also see Ollier's Disease

Exstrophy of the Bladder

• List of Sites

Eye Retraction Syndrome

• See Duane('s) (Retraction) Syndrome

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