Vitamin A deficiency in an infant with PAGOD syndrome

American Journal of Medical Genetics, Part A

Volumn 149, Issue 10, 2009, Pages 2241-2247

  Gavrilova, Ralitza ^a   Babovic, Nikola ^a   Lteif, Aida ^a   Eidem, Benjamin ^a   Kirmani, Salman ^a   Olson, Timothy ^a   Babovic Vuksanovic, Dusica ^a  

^a MAYO CLINIC   (United States)

Author keywords

Agonadism; Dextrocardia; Omphalocele diaphragmatic defect; Pulmonary hypoplasia; Vitamin A deficiency

Indexed keywords

MEMBRANE RECEPTOR; PROTEIN STRA6; RETINOL; UNCLASSIFIED DRUG;

ARTICLE; CASE REPORT; CONGENITAL MALFORMATION; DIAPHRAGM DISEASE; GENITAL MALFORMATION; GONADAL AGENESIS; HUMAN; KARYOTYPE; LUNG HYPOPLASIA; MALE; MATTHEW WOOD SYNDROME; MUELLERIAN DUCT; NEWBORN; OMPHALOCELE; PAGOD SYNDROME; PRIORITY JOURNAL; PULMONARY ARTERY; RETINOL DEFICIENCY; SYNDROME; TESTIS ATROPHY;

ADULT; FATAL OUTCOME; FEMALE; HUMANS; HYPOPLASTIC LEFT HEART SYNDROME; INFANT, NEWBORN; LUNG DISEASES; MALE; PREGNANCY; PRENATAL DIAGNOSIS; SYNDROME; VITAMIN A DEFICIENCY;

ANIMALIA;

EID: 70349514867     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.32998     Document Type: Article

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