Disease Index

Crane-Heise syndrome is a very rare syndrome characterized by poorly mineralized calvarium, facial dysmorphism, vertebral abnormalities and absent clavicles

congenital abnormality in which the meninges protrude through a defect in the cranium

human disease

neuralgia that involves the cranial neuron projection bundle

Cranio-osteoarthropathy (COA) is a form of primary hypertrophic osteoarthropathy (see this term) characterized by delayed closure of the cranial sutures and fontanels, digital clubbing, arthropathy, and periostosis

Craniolenticulosutural dysplasia (CLSD), also known as Boyadjiev-Jabs syndrome, is characterized by the specific association of large and late-closing fontanels, hypertelorism, early-onset cataract and mild generalized skeletal dysplasia

osteosclerosis that results in increased calcium concentration located in skull which decreases the size of cranium foramina and cervical spinal canal

human disease

human disease

human disease

human disease

human disease

osteosclerosis that has material basis in mutations in the ANKH gene which results in progressive thickening located in skull and abnormally shaped ends of long bones in the limbs

Craniomicromelic syndrome is a very rare disorder characterized by intrauterine growth retardation, underossification of the skull with large fontanels, short limbs with absent phalanges and finger and toe syndactyly

type of brain tumor derived from pituitary gland embryonic tissue that occurs most commonly in children, but also affects adults

rare congenital malformation of the central nervous system, and most severe form of neural tube defect in which both the brain and spinal cord remain open to varying degrees

human disease

human disease

premature fusion of bones in the skull

human disease

human disease

medical condition

medical condition