Clinical and neuroradiological features of the 9p deletion syndrome

Child's Nervous System

Volumn 32, Issue 2, 2016, Pages 327-335

  Spazzapan, Peter ^a   Arnaud, Eric ^a   Baujat, Genevieve ^a   Nizon, Mathilde ^a   Malan, Valerie ^a   Brunelle, Francis ^a   Di Rocco, Federico ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

Craniosynostosis; Magnetic resonance; Trigonocephaly

Indexed keywords

ARTICLE; ASTHMA; CAFE AU LAIT SPOT; CHILD; CHROMOSOME 9P; CHROMOSOME DELETION; CLINICAL ARTICLE; COGNITIVE DEFECT; CORPUS CALLOSUM; CORPUS CALLOSUM AGENESIS; COUGHING; EARLY DIAGNOSIS; EPILEPSY; EXOPHTHALMOS; FEMALE; FOOT MALFORMATION; FRONTAL CORTEX; HEART MURMUR; HETEROTOPIA; HUMAN; HYDROCEPHALUS; HYPERTELORISM; HYPOPLASIA; INGUINAL HERNIA; LIMB MALFORMATION; LONG PHILTRUM; MALE; MEDICAL SPECIALIST; MICROGNATHIA; MICROTIA; MIDFACE HYPOPLASIA; MUSCLE HYPOTONIA; NEURORADIOLOGY; NIPPLE MALFORMATION; NUCLEAR MAGNETIC RESONANCE IMAGING; OMPHALOCELE; OPTIC NERVE ATROPHY; OTITIS; PALPEBRAL FISSURE; PRIORITY JOURNAL; PSYCHOMOTOR RETARDATION; RETROSPECTIVE STUDY; RHINITIS; SCOLIOSIS; SEPTUM PELLUCIDUM; SPEECH DELAY; SYLVIAN FISSURE; SYNOSTOSIS; ABNORMALITIES; BRAIN; CASE CONTROL STUDY; CHROMOSOME 9; CRANIOFACIAL MALFORMATION; CRANIOFACIAL SYNOSTOSIS; DEVELOPMENTAL DISORDER; INFANT; PATHOLOGY; WHITE MATTER;

AGENESIS OF CORPUS CALLOSUM; BRAIN; CASE-CONTROL STUDIES; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 9; CORPUS CALLOSUM; CRANIOFACIAL ABNORMALITIES; CRANIOSYNOSTOSES; DEVELOPMENTAL DISABILITIES; HUMANS; INFANT; MAGNETIC RESONANCE IMAGING; RETROSPECTIVE STUDIES; SEPTUM PELLUCIDUM; WHITE MATTER;

EID: 84958101872     PISSN: 02567040     EISSN: 14330350     Source Type: Journal    
DOI: 10.1007/s00381-015-2957-2     Document Type: Article

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