Basal ganglion calcification

The pineal gland, conarium, or epiphysis cerebri, is a small endocrine gland in the brain of most vertebrates. The pineal gland produces melatonin, a serotonin-derived hormone which modulates sleep patterns in both circadian and seasonal cycles. [Source: Wikipedia ]

May Cause
Solitary intracranial calcification
May Be Caused by
Aicardi-Goutiéres syndrome
AIDS
Atherosclerosis
Biotinidase deficiency
Birth anoxia
Birth asphyxia
Birth hypoxia
Carbon monoxide intoxication
Carbonic anhydrase II deficiency
Cardiovascular event
Cerebral calcification Kahn-Markowitz type
Cerebro-oculo-facio-skeletal syndrome
Chickenpox
Cockayne syndrome
Complex neurologic syndrome-mitochondrial DNA mutation
Congenital rubella
Congenital chickenpox
Congenital cytomegalovirus infection
Congenital measles
Coxsackie B
Coxsackie B virus infection
Cysticercosis
Demyelinating disease
Encephalitis
Epstein-Barr virus infection
Fahr disease
Familial hypocalcemia-hypocalciuria
Familial idiopathic basal ganglia calcification
Fetal cytomegalovirus infection
Fetal rubella infection
Fetal toxoplasmosis infection
Fetal varicella infection
Fried syndrome
Hallervorden-Spatz syndrome
Hastings-James syndrome
Hemolytic-uremic syndrome
Hemorrhage
Hyperparathyroidism
Hypoglycemia
Hypoparathyroidism
Hypothyroidism
Hypoxia
Idiopathic
Infantile hypothyroidism
Kearns-Sayre syndrome
Lactic acidemia
Lead encephalopathy
Lead intoxication
Leigh disease
Lipoid proteinosis
Maple syrup urine disease
Measles encephalitis
MELAS syndrome
Methemoglobinopathy
Methotrexate
Mitochondrial disorder
Mitochondrial myopathy
Möbius syndrome
Nephrotic syndrome
Neurofibromatosis
Normal variant
Oculo-dento-osseous dysplasia
Parasitic disease
Parkinsonism
Pearson syndrome
Pertussis
Phenylketonuria
Phenylketonuria variant
Physiologic
Pseudohypoparathyroidism
Pseudopseudohypoparathyroidism
Radiation therapy
Retinitis pigmentosa and basal ganglia calcification
Spondyloenchodrodysplasia
Sturge-Weber syndrome
Systemic lupus erythematosus
Toxoplasmosis
Trisomy 21
Tuberous sclerosis
Aicardi-Goutiéres syndrome
AIDS
Atherosclerosis
Biotinidase deficiency
Birth anoxia
Birth asphyxia
Birth hypoxia
Carbon monoxide intoxication
Carbonic anhydrase II deficiency
Cardiovascular event
Cerebral calcification Kahn-Markowitz type
Cerebro-oculo-facio-skeletal syndrome
Chickenpox
Cockayne syndrome
Complex neurologic syndrome-mitochondrial DNA mutation
Congenital rubella
Congenital chickenpox
Congenital cytomegalovirus infection
Congenital measles
Coxsackie B
Coxsackie B virus infection
Cysticercosis
Demyelinating disease
Encephalitis
Epstein-Barr virus infection
Fahr disease
Familial hypocalcemia-hypocalciuria
Familial idiopathic basal ganglia calcification
Fetal cytomegalovirus infection
Fetal rubella infection
Fetal toxoplasmosis infection
Fetal varicella infection
Fried syndrome
Hallervorden-Spatz syndrome
Hastings-James syndrome
Hemolytic-uremic syndrome
Hemorrhage
Hyperparathyroidism
Hypoglycemia
Hypoparathyroidism
Hypothyroidism
Hypoxia
Idiopathic
Infantile hypothyroidism
Kearns-Sayre syndrome
Lactic acidemia
Lead encephalopathy
Lead intoxication
Leigh disease
Lipoid proteinosis
Maple syrup urine disease
Measles encephalitis
MELAS syndrome
Methemoglobinopathy
Methotrexate
Mitochondrial disorder
Mitochondrial myopathy
Möbius syndrome
Nephrotic syndrome
Neurofibromatosis
Normal variant
Oculo-dento-osseous dysplasia
Parasitic disease
Parkinsonism
Pearson syndrome
Pertussis
Phenylketonuria
Phenylketonuria variant
Physiologic
Pseudohypoparathyroidism
Pseudopseudohypoparathyroidism
Radiation therapy
Retinitis pigmentosa and basal ganglia calcification
Spondyloenchodrodysplasia
Sturge-Weber syndrome
Systemic lupus erythematosus
Toxoplasmosis
Trisomy 21
Tuberous sclerosis