• Thumbnail for Septo-optic dysplasia
    Septo-optic dysplasia (SOD), known also as de Morsier syndrome, is a rare congenital malformation syndrome that features a combination of the underdevelopment...
    11 KB (1,077 words) - 07:23, 15 April 2024
  • and delayed developmental outcome. ONH is often referred to as septo-optic dysplasia, a term that refers to agenesis of the septum pellucidum. It is...
    18 KB (2,204 words) - 01:43, 29 July 2024
  • Thumbnail for Septum pellucidum
    callosum down to the fornix. The septum is not present in the syndrome septo-optic dysplasia. The septum pellucidum is located in the septal area in the midline...
    5 KB (508 words) - 05:16, 26 February 2024
  • Thumbnail for Corpus callosum
    lesion in the splenium, mostly associated with infectious diseases Septo-optic dysplasia Susac's syndrome characterised by lesions as small holes in the...
    31 KB (3,601 words) - 13:08, 30 August 2024
  • dispersal syndrome Senior–Løken syndrome Sensenbrenner syndrome Septo-optic dysplasia Serkal syndrome Serotonin syndrome Serpentine fibula-polycystic...
    42 KB (4,065 words) - 11:33, 29 August 2024
  • Thumbnail for Growth hormone deficiency
    deficiency congenital malformations involving the pituitary (e.g., septo-optic dysplasia, posterior pituitary ectopia) chronic kidney disease intracranial...
    28 KB (3,067 words) - 05:39, 26 June 2024
  • Thumbnail for Hypopituitarism
    and feet, coarse facial features), and if the tumor extends to the optic nerve or optic chiasm, there may be visual field defects. Headaches may also accompany...
    41 KB (4,441 words) - 12:48, 27 March 2024
  • an integrated circuit packaging type Septo-optic dysplasia (SOD), a congenital malformation syndrome of the optic nerve Sphincter of Oddi dysfunction (SOD)...
    2 KB (309 words) - 12:06, 29 August 2024
  • Thumbnail for Hypothyroidism
    congenital disorders, neonatal illness Central: pituitary dysfunction (idiopathic, septo-optic dysplasia, deficiency of PIT1, isolated TSH deficiency)...
    79 KB (8,159 words) - 01:26, 27 August 2024
  • Thumbnail for Coenzyme Q – cytochrome c reductase
    exercise intolerance. Other mutations have been reported to cause septo-optic dysplasia and multisystem disorders. However, mutations in BCS1L, a gene responsible...
    23 KB (2,325 words) - 16:15, 16 July 2024