Laryngeal atresia, encephalocele, and limb deformities (LEL): A possible new syndrome [10]

Journal of Medical Genetics

Volumn 38, Issue 6, 2001, Pages 420-422

  Kalache, K D ^a   Masturzo, B ^a   Scott, R J ^a   Rodeck, C H ^a   Chitty, L S ^a  

^a CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ASCITES; ASYSTOLE; ATRESIA; CASE REPORT; DISEASE CLASSIFICATION; ENCEPHALOCELE; FETUS; FETUS DISEASE; HUMAN; LARYNX DISORDER; LETTER; LIMB MALFORMATION; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; CYSTIC ADENOMATOID MALFORMATION OF LUNG, CONGENITAL; DIAGNOSIS, DIFFERENTIAL; ENCEPHALOCELE; FEMALE; FETUS; HUMANS; LARYNX; LIMB DEFORMITIES, CONGENITAL; SYNDROME;

EID: 0034988862     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (9)

1. Fetus with asymmetric parietal encephalocele, and hydrops secondary to laryngeal atresia
2. Congenital abnormalities associated with limb deficiency defects: A population study based on cases from the Hungarian Congenital Malformation Registry (1975-1984)
3. "ADAM complex" (amniotic deformity, adhesions, mutilations) - A pattern of craniofacial and limb defects
4. Congenital high airway obstruction syndrome (CHAOS): A potential for perinatal intervention
5. Prenatal diagnosis of laryngeal atresia in two cases of congenital high airway obstruction syndrome (CHAOS)
6. Laryngeal atresia - A cause of hydrops fetalis
7. Prenatal diagnosis of laryngeal atresia
8. Ectopic neuroglial tissue associated with intrapulmonary congenital cystic adenomatoid malformation
9. Complexities of limb anomalies: The lower extremity in the "prune belly" phenotype