optic_nerve_hypoplasia

Optic Nerve Hypoplasia

  • Abnormally small optic nerve head
  • Congenital decrease optic nerve fibers

Septo Optic Dysplasia - any combination of optic nerve hypoplasia, pituitary gland hypoplasia and midline brain abnormalities

  • One of leading causes of childhood blindness
  • Incidence
  • Young maternal age
  • First parity
  • Maternal smoking
  • Preterm birth

Clinical Features

  • Peripapillary ring- “Double ring sign”
  • Small optic nerve
  • Thinning of the nerve fiber layer
  • Possible tortuosity of retinal vasculature
  • Possible persistent grey appearance of the nerve

Optic Nerve Measurements

  • 11 rare single nucleotide variants were identified in 10 persons (34%) in one 2020 study, including:
    • 2 variants in COL4A1
    • 2 variants in COL4A2
    • 2 variants in CYP26C1
    • 1 variant in each of OPA1 (in a patient who also had a COL4A1 variant), KIF7, SPG7, CYP26A1, and UBE3B
    • 1 copy number variant was identified in SOX5 in 1 patient

See PLoS One 2020;15(2):e0228622

  • Brain Anomalies
    • More common
      • Microcephly, absent septum pellucid, posterior pituitary ectopia, migrational anomalies (hypoplasia of corpus callous)
    • Less common
      • porencephaly, schizencephaly, arachnoid cyst, epidermoid cyst
  • Pituitary Dysfunction
    • neonatal hypoglycemia
      • associated with neonatal cholestatic jaundice, convulsions and or coma after anesthesia
    • growth hormone deficency
    • diabetes insipidus
  • olfactory hypoplasia

In Olmstead County, MD population

  • Premature birth- 32%
  • Maternal diabetes- 16%
  • Bilateral- 84%
  • Developmental Delay- 63%
  • Neurologic defects- 53%
    • Microcephaly (16%)
    • Cerebral palsy (16%)
    • Corpus callous hypoplasia (11%)
    • Septum Pellucidum aplasia (11%)
    • White matter hypoplasia (11%)
    • Hydrocephalus (11%)
    • Decreased visual acuity- 47%
    • Strabismus- 42%
      • Esotropia 21%
      • Exotropia 21%
    • Endocrine dysfunction- 26%
      • Growth hormone deficiency (16%)
      • Hypothyroid (16%)
      • Diabetes insipidus (11%)
      • Adrenal insufficiency (5%)
      • Hypopituitarism (5%)
      • Precocious puberty (5%)
    • Nystagmus- 26%
    • Refractive error can be myopia, hyperopia and or astigmatism
    • Amblyopia- 11%
  • Dominant inheritance
  • Prenatal Drug exposure
  • Chromosome abnormalities
    • Distal 5q deletion syndrome
    • Chromsome 1 anomaly- Muscle eye brain disease
    • Partial deletion chromosome 6p
    • Chromosome 7(q22→q34) and 7q32-34 interstitial duplication
    • Chromosome 17 interstitial deletion
  • Frontonasal dysplasia
  • Idiopathic growth hormone deficiency (ONH seen in 9%)
  • Nevus sebaceous of Jadassohn (cutaneous, possibly malignant, phacomatosis)
  • Maternal Diabetes
  • Orbital hemangioma
  • Periventricular leukomalacia
  • Suprasellar teratoma

Resources

  • optic_nerve_hypoplasia.txt
  • Last modified: 2025/01/12 15:19
  • by oculoman