Congenital mydriasis and prune belly syndrome in a child with an ACTA2 mutation

Journal of AAPOS

Volumn 18, Issue 4, 2014, Pages 393-395

  Brodsky, Michael C ^a   Turan, Kadriye Erkan ^b   Khanna, Cheryl L ^a   Patton, Alice ^a   Kirmani, Salman ^a  

^a MAYO CLINIC   (United States)

^b HACETTEPE UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

ACTA2 PROTEIN; ALPHA ACTIN; UNCLASSIFIED DRUG; ALPHA ACTININ 2; ACTA2 PROTEIN, HUMAN; ACTIN;

ARTICLE; BIOMICROSCOPY; CASE REPORT; CEREBROVASCULAR MALFORMATION; CHILD; CONGENITAL MALFORMATION; CONGENITAL MYDRIASIS; ECHOCARDIOGRAPHY; EYE EXAMINATION; GENE MUTATION; GONIOSCOPY; HUMAN; MALE; MYDRIASIS; PRIORITY JOURNAL; PRUNE BELLY SYNDROME; REFRACTION ERROR; RETINOSCOPY; SCHOOL CHILD; SLIT LAMP; VISUAL ACUITY; ACCOMMODATION PARALYSIS; CRYPTORCHISM; HEART ATRIUM SEPTUM DEFECT; HYDRONEPHROSIS; HYDROURETER; OLIGOHYDRAMNIOS; UROLOGICAL PROCEDURE; CEREBROVASCULAR DISEASE; EYE DISEASE; GENETICS; MAGNETIC RESONANCE ANGIOGRAPHY; POINT MUTATION;

ACTINS; CEREBROVASCULAR DISORDERS; CHILD; ECHOCARDIOGRAPHY; EYE DISEASES, HEREDITARY; HUMANS; MAGNETIC RESONANCE ANGIOGRAPHY; MALE; MYDRIASIS; POINT MUTATION; PRUNE BELLY SYNDROME; RETINOSCOPY; VISUAL ACUITY;

EID: 84925884630     PISSN: 10918531     EISSN: 15283933     Source Type: Journal    
DOI: 10.1016/j.jaapos.2014.02.010     Document Type: Article

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