Literature DB >> 985032

[Hypopituitarism with hypoplasia of the optic nerve (Kaplan, Grumbach and Hoyt syndrome].

J E Toublanc, J L Chaussain, C Lejeune, F De Paillerets, J C Job.   

Abstract

Two new cases of the syndrome described by Kaplan, Grumbach and Hoyt are reported. The two children were hypopituitary dwarfs, with congenital nystagmus and small optic discs with double border. Pneumoencephalography showed malformations of the median structures, with trans-sphenoidal encephalocele in one case. The definition of this syndrome and its relation to De Morsier's septooptical dysplasia are briefly discussed.

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Year:  1976        PMID: 985032

Source DB:  PubMed          Journal:  Arch Fr Pediatr        ISSN: 0003-9764


  5 in total

1.  Lateral frontal encephalocele associated with dysplasia of orbit, eyeball, and eyelid.

Authors:  A Kulali; O Rahmanli
Journal:  Childs Nerv Syst       Date:  1990-01       Impact factor: 1.475

2.  Cephaloceles: clinical and neuroradiological appearance. Associated cerebral malformations.

Authors:  C Diebler; O Dulac
Journal:  Neuroradiology       Date:  1983       Impact factor: 2.804

Review 3.  Optic nerve hypoplasia: septo-optic-pituitary dysplasia syndrome.

Authors:  T E Acers
Journal:  Trans Am Ophthalmol Soc       Date:  1981

4.  Pituitary function in a patient with septo-optic dysplasia and pituitary dwarfism (Kaplan-Grumbach-Hoyt syndrome).

Authors:  M K Lovrencić; V Oberiter; Z R Banovac; L Schmutzer; M Petek
Journal:  Eur J Pediatr       Date:  1978-08-17       Impact factor: 3.183

5.  Endocrine optic neuropathies.

Authors:  F Moro; F Drago
Journal:  Doc Ophthalmol       Date:  1980-10-15       Impact factor: 2.379

  5 in total

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