Idiopathic familial basal ganglia calcification associated with juvenile hypertension.
نویسندگان
چکیده
منابع مشابه
Cooccurrence of Multiple Sclerosis and Idiopathic Basal Ganglia Calcification
Multiple sclerosis (MS) is a chronic inflammatory demyelinating and neurodegenerative disease of central nervous system that affects both white and gray matter. Idiopathic calcification of the basal ganglia is a rare neurodegenerative disorder of unknown cause that is characterized by sporadic or familial brain calcification. Concurrence of multiple sclerosis (MS) and idiopathic basal ganglia c...
متن کاملFamilial idiopathic basal ganglia calcification (Fahr’s disease)
Familial idiopathic basal ganglia calcification (Fahr`s disease) is a rare neurodegenerative disorder characterized by symmetrical and bilateral calcification of the basal ganglia. Calcifications may also occur in other brain regions such as dentate nucleus, thalamus, and cerebral cortex. Both familial and non-familial cases of Fahr`s disease have been reported, predominantly with autosomal-dom...
متن کاملFamilial idiopathic basal ganglia calcification: rediscovering an old challenge in organic psychiatric disorders.
Familial idiopathic basal ganglia calcification: rediscovering an old challenge in organic psychiatric disorders João Ricardo Mendes de Oliveira, Matheus Fernandes de Oliveira Keizo Asami Laboratory (LIKA), Universidade Federal de Pernambuco (UFPE), Recife, PE, Brazil. Neuropsychiatric Department, UFPE, Recife, PE, Brazil. Neurosurgery Residency Program, Hospital do Servidor Público Estadual de...
متن کاملBasal ganglia calcification in idiopathic hypoparathyroidism
ABSTRACT: Hypoparathyroidism refers to a group of disorders in which extracellular calcium levels cannot be maintained within the normal range due to relative or absolute deficiency of parathyroid hormone. Clinically, hypoparathyroidism manifests predominantly as neuromuscular dysfunction caused by hypocalcemia. Basal ganglia calcification in particular is associated with hypoparathyroidism. Tw...
متن کاملMutation Analysis of SLC20A2 and SPP2 as Candidate Genes for Familial Idiopathic Basal Ganglia Calcification
BACKGROUND Familial Idiopathic Basal Ganglia Calcification (IBGC) is a rare neurodegenerative disorder which is usually transmitted as an autosomal dominant trait. IBGC is genetically heterogeneous and SLC20A2, on chromosome 8p21.1-8q11.23, is the first gene found in IBGC-affected patients with varied ancestry. On the other hand, several candidate genes for IBGC on chromosome 2q37, including th...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Journal of neurology, neurosurgery, and psychiatry
دوره 43 3 شماره
صفحات -
تاریخ انتشار 1980