MRI of the hypophysis in a patient with the 18q- syndrome

Neuroradiology

Volumn 43, Issue 10, 2001, Pages 875-876

  Bekiesiaska Figatowska M ^a   Walecki, J ^b  

^a Central Railway Hospital Warsaw   (Poland)

^b MEDICAL CENTER FOR POSTGRADUATE EDUCATION   (Poland)

Author keywords

18q syndrome; Empty sella; Hypophysis; Magnetic resonance imaging

Indexed keywords

ADENOHYPOPHYSIS; ARTICLE; BRAIN VENTRICLE DILATATION; CASE REPORT; CEREBROSPINAL FLUID; CHROMOSOME 18Q; CLINICAL FEATURE; CORPUS CALLOSUM; FEMALE; HUMAN; HYPOPLASIA; MALFORMATION SYNDROME; NUCLEAR MAGNETIC RESONANCE IMAGING; PRESCHOOL CHILD; PRIORITY JOURNAL; SELLA TURCICA;

ABNORMALITIES, MULTIPLE; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 18; DEAFNESS; FACIAL BONES; FEMALE; GENE DELETION; GROWTH DISORDERS; HEART DEFECTS, CONGENITAL; HUMANS; MAGNETIC RESONANCE IMAGING; MENTAL RETARDATION; PITUITARY GLAND; SYNDROME;

EID: 0034780508     PISSN: 00283940     EISSN: None     Source Type: Journal    
DOI: 10.1007/s002340100578     Document Type: Article

References (6)

1. Magnetic resonance imaging demonstrates incomplete myelination in 18q- syndrome: Evidence for myelin basic protein haploinsufficiency
2. White matter changes associated with deletions of the long arm of chromosome 18 (18q- syndrome): A dysmyelinating disorder?
3. Delayed myelination in a patient with 18q- syndrome
4. Neurologic manifestations in 18q-syndrome
5. Segmental spinal muscular atrophy and dermatological findings in a patient with chromosome 18q deletion
6. Magnetic resonance of myelin, myelination, and myelin disorders