Aplasia cutis congenita, terminal limb defects and falciform retinal folds: Confirmation of a distinct syndrome of vascular disruption

Clinical Dysmorphology

Volumn 16, Issue 1, 2007, Pages 39-41

  Prothero, Joanna ^a   Nicholl, Richard ^a   Wilson, Judith ^a   Wakeling, Emma L ^a,b  

^a EALING HOSPITAL NHS TRUST   (United Kingdom)

^b London North West University Health Care NHS Trust   (United Kingdom)

Author keywords

Adams Oliver syndrome; Aplasia cutis; Autosomal recessive; Distal phalangeal hypoplasia; Retinal detachment

Indexed keywords

ADAMS OLIVER SYNDROME; ARTICLE; AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; CLINICAL FEATURE; DIAGNOSTIC ACCURACY; HUMAN; IMAGE ANALYSIS; INFANT; LIMB DEFECT; MALE; NEWBORN; NUCLEAR MAGNETIC RESONANCE IMAGING; PHALANX HYPOPLASIA; PRIORITY JOURNAL; RETINA FOLD; SKIN APLASIA; SYMPTOM; VASCULAR DISEASE;

ADULT; ECTODERMAL DYSPLASIA; FEMALE; GENES, RECESSIVE; HUMANS; INFANT; LIMB DEFORMITIES, CONGENITAL; MALE; RETINA; SYNDROME; VASCULAR DISEASES;

EID: 33845600215     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/MCD.0b013e328010b81c     Document Type: Article

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