Severe Peters Plus syndrome-like phenotype with anterior eye staphyloma and hypoplastic left heart syndrome: Proposal of a new syndrome

Congenital Anomalies

Volumn 50, Issue 3, 2010, Pages 197-199

  Shimizu, Reiko ^a   Saito, Ryota ^b   Hoshino, Kenji ^b   Ogawa, Kiyoshi ^b   Negishi, Takashi ^c   Nishimura, Jiro ^c   Mitsui, Norimasa ^c   Osawa, Makiko ^a   Ohashi, Hirofumi ^c  

^a TOKYO WOMEN'S MEDICAL UNIVERSITY   (Japan)

^b Division of Cardiology   (Japan)

^c SAITAMA CHILDREN'S MEDICAL CENTER   (Japan)

Author keywords

anterior staphyloma; hypoplastic left heart syndrome; Peters anomaly; Peters Plus syndrome

Indexed keywords

BETA 1,3 GLUCOSYLTANSFERASE; GLUCOSYLTRANSFERASE; UNCLASSIFIED DRUG;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; B3GALTL GENE; CASE REPORT; CHROMOSOME ANALYSIS; CLEFT LIP PALATE; CORNEA OPACITY; ECHOCARDIOGRAPHY; FEMALE; GENE MUTATION; HUMAN; HYPOPLASTIC LEFT HEART SYNDROME; NEWBORN; PETERS ANOMALY; PETERS PLUS SYNDROME; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; CORNEA; FATAL OUTCOME; FEMALE; GALACTOSYLTRANSFERASES; GLUCOSYLTRANSFERASES; GROWTH DISORDERS; HUMANS; HYPOPLASTIC LEFT HEART SYNDROME; INFANT, NEWBORN; LIMB DEFORMITIES, CONGENITAL;

EID: 77956017877     PISSN: 09143505     EISSN: 17414520     Source Type: Journal    
DOI: 10.1111/j.1741-4520.2010.00282.x     Document Type: Article

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