Evidence for possible Mendelian inheritance of septo-optic dysplasia

Acta Paediatrica, International Journal of Paediatrics

Volumn 85, Issue 3, 1996, Pages 391-392

  Wales, J K H ^a,c   Quarrell, O W J ^b  

^a SHEFFIELD CHILDREN S HOSPITAL   (United Kingdom)

^b Centre for Human Genetics   (United Kingdom)

^c UNIVERSITY OF SHEFFIELD   (United Kingdom)

Author keywords

Inheritance; Recurrence risk; Septo optic dysplasia

Indexed keywords

ARTICLE; BRAIN MALFORMATION; CASE REPORT; CONSANGUINITY; FEMALE; HUMAN; HYPOPITUITARISM; INHERITANCE; MALE; NEWBORN; PEDIGREE; PRIORITY JOURNAL; RECURRENT DISEASE; SEPTOOPTIC DYSPLASIA; SIBLING;

EID: 0029967477     PISSN: 08035253     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1651-2227.1996.tb14044.x     Document Type: Article

References (6)

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2. Smith PJ, Hindmarsh P, Kendall B, Brook CGD. Dysgenesis of the corpus callosum and hypopituitarism. Acta Paediatr Scand 1986;75:923-6
3. McKusick VA. Mendelian inheritance in man. 10th ed. Baltimore, John Hopkins University Press, 1992
4. Blethen SL, Weldon VV. Hypopituitarism and septo-optic "dysplasia" in first cousins. Am J Med Genet 1985;21:123-9
5. Benner JD, Preslan MW, Gratz E, Joslyn J, Schwartz M, Kelman S. Septo-optic dysplasia in two siblings. Am J Ophthalmol 1990;109:632-7
6. Young ID, Trounce JQ, Levene MI, Fitzsimmons JS, Moore JR. Agenesis of the corpus callosum and microcephaly in siblings. Clin Genet 1985;28:225-30