Intracranial calcification

Atherosclerosis is a disease in which the wall of the artery develops abnormalities, called lesions. These lesions may lead to narrowing due to the buildup of atheromatous plaque. [Source: Wikipedia ]

May Cause
Intracranial lesion in an infant
May Be Caused by
Aicardi-Goutiéres syndrome
AIDS
Arterial calcification of infancy
Autosomal recessive congenital intrauterine infection-like syndrome
Bannayan-Riley-Ruvalcaba syndrome
Baraitser-Reardon syndrome
Biotinidase deficiency
Birth asphyxia
Blue rubber bleb nevus syndrome
Brachyolmia
Brain dysgenesis-focal calcification
Breathnach syndrome
Calcinosis
Carbonic anhydrase II deficiency
Cardiac surgery
Celiac disease
Cerebral calcification Kahn-Markowitz type
Cerebro-oculo-facio-skeletal syndrome
Cerebrofaciothoracic dysplasia
Coats-plus syndrome
Cockayne syndrome
Craniosynostosis - intracranial calcifications
Crome syndrome
Cysticercosis
Cystinosis
Diastrophic dysplasia
Disseminated hemangiomatosis
Dyskeratosis congenita
Dysosteosclerosis
Encephalocraniocutaneous lipomatosis
Epidermal nevus syndrome
Fahr disease
Familial hidrotic ectodermal dysplasia
Familial idiopathic symmetric basal ganglia calcification and microcephaly
Familial occipital calcification and epilepsy
Fetal cytomegalovirus infection
Fetal herpes simplex infection
Fetal rubella infection
Fetal toxoplasmosis infection
Fetal varicella infection
Fowler syndrome
Gorlin syndrome
Hallermann-Streiff syndrome
Hastings-James syndrome
Homocystinuria
Hyperlipoproteinemia
Hyperparathyroidism
Hypervitaminosis D
Hypodipsic hypernatremia
Hypoparathyroidism
Hypopituitarism
Hypothyroidism
Hypoxia-ischemia
Idiopathic fetal encephalopathy
Increased renal phosphate reabsorption
Infantile familial encephalopathy with cerebral calcification and leukodystrophy
Kallmann syndrome
Kearns-Sayre syndrome
Klippel-Trénaunay-Weber syndrome
Lead intoxication
Lethal osteosclerotic skeletal dysplasia
Lipodystrophy
Lipoid proteinosis
Lipomembranous polycystic osteodysplasia
Lissencephaly
Maffucci syndrome
Marinesco-Sjögren syndrome
Marshall syndrome
Measles encephalitis
MELAS syndrome
Membranous lipodystrophy
Meningioangiomatosis
Meningitis
Metastatic calcification
Methotrexate
Microcephaly - microphthalmia - cataract - intracranial calcification
Miller-Dieker syndrome
Mitochondrial encephalomyopathy
Multiple carboxylase deficiency
Nephrogenic diabetes insipidus - intracranial calcification
Neu-Laxova syndrome
Neurocutaneous melanosis sequence
Neurofibromatosis type 1
Neurofibromatosis type 2
Oculo-auriculo-vertebral spectrum
Oculo-dento-osseous dysplasia
Papillon-Lefèvre syndrome
Parkinson disease
Pelizaeus-Merzbacher disease
Phenylketonuria
Pituitary stone
Polyglandular autoimmune disease
Porphyria
Pseudohypoparathyroidism
Pseudoxanthoma elasticum
Radiation therapy
Rambaud-Galian syndrome
Retinitis pigmentosa and basal ganglia calcification
Romberg syndrome
Short rib-polydactyly syndrome type 3
Spondyloenchodrodysplasia
Sturge-Weber syndrome
Sulfite oxidase deficiency
Systemic lupus erythematosus
Tolmie syndrome
Trisomy 21
Troost syndrome
Tuberous sclerosis
Tubular stenosis dyplasia
Twin-to-twin transfusion syndrome
Von Hippel-Lindau disease
Weismann-Netter syndrome
West syndrome
Williams syndrome
Wilson disease
Aicardi-Goutiéres syndrome
AIDS
Arterial calcification of infancy
Autosomal recessive congenital intrauterine infection-like syndrome
Bannayan-Riley-Ruvalcaba syndrome
Baraitser-Reardon syndrome
Biotinidase deficiency
Birth asphyxia
Blue rubber bleb nevus syndrome
Brachyolmia
Brain dysgenesis-focal calcification
Breathnach syndrome
Calcinosis
Carbonic anhydrase II deficiency
Cardiac surgery
Celiac disease
Cerebral calcification Kahn-Markowitz type
Cerebro-oculo-facio-skeletal syndrome
Cerebrofaciothoracic dysplasia
Coats-plus syndrome
Cockayne syndrome
Craniosynostosis - intracranial calcifications
Crome syndrome
Cysticercosis
Cystinosis
Diastrophic dysplasia
Disseminated hemangiomatosis
Dyskeratosis congenita
Dysosteosclerosis
Encephalocraniocutaneous lipomatosis
Epidermal nevus syndrome
Fahr disease
Familial hidrotic ectodermal dysplasia
Familial idiopathic symmetric basal ganglia calcification and microcephaly
Familial occipital calcification and epilepsy
Fetal cytomegalovirus infection
Fetal herpes simplex infection
Fetal rubella infection
Fetal toxoplasmosis infection
Fetal varicella infection
Fowler syndrome
Gorlin syndrome
Hallermann-Streiff syndrome
Hastings-James syndrome
Homocystinuria
Hyperlipoproteinemia
Hyperparathyroidism
Hypervitaminosis D
Hypodipsic hypernatremia
Hypoparathyroidism
Hypopituitarism
Hypothyroidism
Hypoxia-ischemia
Idiopathic fetal encephalopathy
Increased renal phosphate reabsorption
Infantile familial encephalopathy with cerebral calcification and leukodystrophy
Kallmann syndrome
Kearns-Sayre syndrome
Klippel-Trénaunay-Weber syndrome
Lead intoxication
Lethal osteosclerotic skeletal dysplasia
Lipodystrophy
Lipoid proteinosis
Lipomembranous polycystic osteodysplasia
Lissencephaly
Maffucci syndrome
Marinesco-Sjögren syndrome
Marshall syndrome
Measles encephalitis
MELAS syndrome
Membranous lipodystrophy
Meningioangiomatosis
Meningitis
Metastatic calcification
Methotrexate
Microcephaly - microphthalmia - cataract - intracranial calcification
Miller-Dieker syndrome
Mitochondrial encephalomyopathy
Multiple carboxylase deficiency
Nephrogenic diabetes insipidus - intracranial calcification
Neu-Laxova syndrome
Neurocutaneous melanosis sequence
Neurofibromatosis type 1
Neurofibromatosis type 2
Oculo-auriculo-vertebral spectrum
Oculo-dento-osseous dysplasia
Papillon-Lefèvre syndrome
Parkinson disease
Pelizaeus-Merzbacher disease
Phenylketonuria
Pituitary stone
Polyglandular autoimmune disease
Porphyria
Pseudohypoparathyroidism
Pseudoxanthoma elasticum
Radiation therapy
Rambaud-Galian syndrome
Retinitis pigmentosa and basal ganglia calcification
Romberg syndrome
Short rib-polydactyly syndrome type 3
Spondyloenchodrodysplasia
Sturge-Weber syndrome
Sulfite oxidase deficiency
Systemic lupus erythematosus
Tolmie syndrome
Trisomy 21
Troost syndrome
Tuberous sclerosis
Tubular stenosis dyplasia
Twin-to-twin transfusion syndrome
Von Hippel-Lindau disease
Weismann-Netter syndrome
West syndrome
Williams syndrome
Wilson disease