A new syndrome with craniofacial and skeletal dysmorphisms and developmental delay

Clinical Dysmorphology

Volumn 10, Issue 2, 2001, Pages 87-93

  Der Kaloustian, Vazken M ^a,b,c   Pelletier, Myriam ^a,b,c   Costa, Teresa ^a,b,c   Blackston, Dwain R ^a,b,c   Oudjhane, Kamaldine ^a,b,c  

^a MONTREAL CHILDREN S HOSPITAL   (Canada)

^b DALHOUSIE UNIVERSITY   (Canada)

^c EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Epilepsy; Hallux; Hydronephrosis; Hypertelorism; Macrostomia; Malformations; Pterygia; Trigonocephaly

Indexed keywords

ADOLESCENT; ARTICLE; BRACHYCEPHALY; CASE REPORT; CLINICAL EXAMINATION; CRANIOFACIAL MALFORMATION; DEVELOPMENTAL DISORDER; EAR MALFORMATION; FACE DYSMORPHIA; HUMAN; HYPERTELORISM; MACROSTOMIA; MALE; MALFORMATION SYNDROME; MICROGNATHIA; NOSE MALFORMATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PACHYGYRIA; PRIORITY JOURNAL; PTERYGIUM; SYNDROME DELINEATION; UMBILICAL HERNIA; VARUS DEFORMITY;

EID: 0035086381     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-200104000-00003     Document Type: Article

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1. A new syndrome with craniofacial and skeletal dysmorphisms and developmental delay
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7. Hypertelorism, proptosis, polysyndactyly, hypospadias and normal height in 3 sibs: A new syndrome?
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9. Trigonocephaly and the Opitz C syndrome
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11. Natural history of the recombinant (8) syndrome
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