Sudden death in septo-optic dysplasia: Report of 5 cases

Archives of Ophthalmology

Volumn 115, Issue 1, 1997, Pages 66-70

  Brodsky, Michael C ^a,e   Conte, Felix A ^c   Taylor, David ^d   Hoyt, Creig S ^c   Mrak, Robert E ^a,b  

^a UNIVERSITY OF ARKANSAS FOR MEDICAL SCIENCES   (United States)

^b DEPARTMENT OF VETERANS AFFAIRS   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

^d GREAT ORMOND STREET HOSPITAL   (United Kingdom)

^e ARKANSAS CHILDREN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADRENAL CORTEX INSUFFICIENCY; ARTICLE; CAUSE OF DEATH; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; CORPUS CALLOSUM; CORTICOTROPIN DEFICIENCY; DISEASE ASSOCIATION; FEMALE; HUMAN; INFANT; MALE; NEWBORN; OPTIC NERVE HYPOPLASIA; PRESCHOOL CHILD; PRIORITY JOURNAL; RISK ASSESSMENT; SEPTUM PELLUCIDUM; SUDDEN DEATH;

EID: 0031022841     PISSN: 00039950     EISSN: None     Source Type: Journal    
DOI: 10.1001/archopht.1997.01100150068011     Document Type: Article

References (30)

1. de Morsier G. Etudes sur les dysraphies crânio-encáphaliques, III: agénésie du septum lucidum avec malformation du tractus optique: la dysplasie septo-optique. Schweiz Arch Neurol Neurochir Psychiatr. 1956;77:267-292.
2. Hoyt WF, Kaplan SL, Grumbach MM, et al. Septo-optic dysplasia and pituitary dwarfism. Lancet. 1970;2:893-894.
3. Brodsky MC, Glasier CM. Optic nerve hypoplasia: clinical significance of associated central nervous system abnormalities on magnetic resonance imaging. Arch Ophthalmol. 1993;111:66-74.
4. Lemire RJ, Loeser JD, Leech RW, Alvord EC Jr. Normal and Abnormal Development of the Human Nervous System. New York, NY: Harper & Row Publishers Inc; 1975.
5. Huseman CA, Kelch RP, Hopwood NJ, et al. Sexual precocity in association with septo-optic dysplasia and hypothalamic hypopituitarism. J Pediatr. 1978;92:748-753.
6. Zaias B, Becker D. Septo-optic dysplasia: developmental or acquired abnormality? a case report. Trans Am Neurol Assoc. 1978;103:273-277.
7. Benoit Gonin JJ, David M, Feit JP, et al. La dysplasie septo-optique avec déficit en hormone antidiurétique et insufficance surrénale central. Nouv Presse Med. 1978;7:3327-3331.
8. Greenfield PS, Wilcox LM, Weiter JJ, Adelman L. Hypoplasia of the optic nerve in association with porencephaly. J Pediatr Ophthalmol Strabismus. 1980;17:75-80.
9. Donat JGF: Septo-optic dysplasia in an infant of a diabetic mother. Arch Neurol. 1981;38:590-591.
10. Michaud J, Mizrabi EM, Urich H. Agenesis of the vermis with fusion of the cerebellar hemispheres, septo-optic dysplasia and associated anomalies. Acta Neuropathol. 1982;56:161-166.
11. Kobori JA, Herrick MK, Urich H. Arrhinencephaly: the spectrum of associated malformations. Brain. 1987;110:237-260.
12. Patel H, Tze WJ, Crichton JU, et al. Optic nerve hypoplasia with hypopituitarism. AJDC. 1975;129:175-180.
13. Roessmann U, Velasco ME, Small EJ, Hori A. Neuropathology of 'septo-optic dysplasia' (de Morsier syndrome) with immunohistochemical studies of the hypothalamus and pituitary gland. J Neuropathol Exp Neurol. 1987;46:597-608.
14. Costello JM, Gluckman PD. Neonatal hypopituitarism: a neurological perspective. Dev Med Child Neurol. 1988;30:190-199.
15. Coulter CL, Leech RW, Schaefer GB, et al. Midline cerebral dysgenesis, dysfunction of the hypothalamic-pituitary axis, and fetal alcohol effects. Arch Neurol. 1993;50:771-775.
16. Werbel SS, Ober KP. Acute adrenal insufficiency. Endocrinol Metabol Clin North Am. 1993;22:303-328.
17. Cross KW, Hey DL, Kennaird DL, et al. Lack of temperature control in infants with abnormalities of the central nervous system Arch Dis Child. 1971;46:437-446.
18. Karch SB, Urich H. Occipital encephalocele: a morphological study. J Neurol Sci. 1972;15:89-112.
19. Kyllerman M, Bager B, Bensch B, et al. Dyskinetic cerebral palsy, I: clinical categories, associated neurological abnormalities, and incidences. Acta Paediatr Scand 1982;71:543-550.
20. Cooper PE. Disorders of the hypothalamus and pituitary gland. In: Joynt RJ, ed. Clinical Neurology. Philadelphia, Pa: JB Lippincott, 1991;3:1-116.
21. Shapiro WR, Williams GH, Plum F. Spontaneous recurrent hypothermia ac- companying agenesis of the corpus callosum. Brain. 1969;92:423-436.
22. Guihard J, Velot-Lerou A, Poitrat C, et al. Hypothermie spontanée récidvante avec agénésie du corps calleux: syndrome de Shapiro (nouvelle observation). Ann Pediatr. 1971;18:645-656.
23. Noël P, Hubert JP, Ectors M, et al. Agenesis of the corpus callosum associated with relapsing hypothermia: a clinico-pathological report. Brain. 1973;96:359-368.
24. Kaufman LM, Miller MT, MaFee MR. Magnetic resonance imaging of pituitary stalk hypoplasia: a discrete midline anomaly associated with endocrine abnormalities in septo-optic dysplasia. Arch Ophthalmol. 1989;107:1485-1489.
25. Kucharczyk W, Lenkinski R, Kucharczyk J, Henkelman RM. The effect of phospholipid vesicles on the NMR relaxation of water: an explanation for the MR appearance of the neurohypophysis? AJNR Am J Neuroradiol. 1990;11:693-700.
26. Kelly WM, Kucharczyk W, Kucharczyk J, et al. Posterior pituitary ectopia: an MR feature of pituitary dwarfism. Am J Neuroradiol. 1988;9:453-460.
27. 1 signal on magnetic resonance imaging: implications for anterior pituitary hormone dysfunction. AJDC. 1993;147:647-652.
28. Taback SP, Dean HJ, and Members of the Canadian Growth Hormone Advisory Comittee. Mortality in Canadian children with growth hormone (GH) deficiency receiving GH therapy 1967-1992. J Clin Endocrinol Metab. 1996;81:1693-1696.
29. Hintz RL. Eternal vigilance: mortality in children with growth hormone deficiency. J Clin Endocrinol Metab. 1996;81:1691-1693.
30. Sherlock DA, McNicol LR. Anaesthesia and septo-optic dysplasia: implications of missed diagnosis in the peri-operative period. Anaesthesia. 1987;42:1302-1305.