Fryns syndrome without diaphragmatic hernia. Report on a new case and review of the literature

Genetic Counseling

Volumn 16, Issue 4, 2005, Pages 363-370

  Alessandri, Jean Luc ^a,b   Brayer, C ^a   Attali, T ^a   Samperiz, S ^a   Tiran Rajaofera, I ^a   Ramful, D ^a   Pilorget, H ^a  

^a CENTRE HOSPITALIER   (France)

^b Centre Hospitalier Departemental Felix Guyon   (France)

Author keywords

Congenital diaphragmatic hernia; Fryns syndrome; Nitrofen; Pulmonary hypoplasia

Indexed keywords

NITROFEN; SURFACTANT;

AUTOSOMAL RECESSIVE DISORDER; CARDIOVASCULAR MALFORMATION; CASE REPORT; CENTRAL NERVOUS SYSTEM MALFORMATION; CLINICAL FEATURE; COARSE FACE; DIAPHRAGM HERNIA; DISTAL LIMB HYPOPLASIA; FRYNS SYNDROME; GASTROINTESTINAL MALFORMATION; HUMAN; HYPOPLASIA; INCIDENCE; LIMB MALFORMATION; LUNG HYPOPLASIA; LUNG MALFORMATION; MALE; NEWBORN; REVIEW; UROGENITAL TRACT MALFORMATION; ANAMNESIS; ARTIFICIAL VENTILATION; CATARACT; ECHOENCEPHALOGRAPHY; HYPOXEMIA; MEDICAL LITERATURE; RESPIRATORY DISTRESS SYNDROME; SKELETON MALFORMATION; THORAX RADIOGRAPHY;

ABNORMALITIES, MULTIPLE; FACIAL BONES; FATAL OUTCOME; FETAL GROWTH RETARDATION; FINGER PHALANGES; GENES, RECESSIVE; GESTATIONAL AGE; HEART SEPTAL DEFECTS, VENTRICULAR; HERNIA, DIAPHRAGMATIC; HUMANS; INFANT, NEWBORN; MALE; SYNDROME;

EID: 30444443448     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (28)

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