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Tuberous Sclerosis: more books (38)

21st Century Complete Medical Guide to Tuberous Sclerosis (TSC): Authoritative Government Documents, Clinical References, and Practical Information for Patients and Physicians by PM Medical Health News, 2004-10
The Official Patient's Sourcebook on Tuberous Sclerosis
Tuberous Sclerosis Complex (Developmental Perspectives in Psychiatry)
Tuberous Sclerosis
Tuberous Sclerosis and Allied Disorders: Clinical, Cellular, and Molecular Studies (Annals of the New York Academy of Sciences) by William G. Johnson, 1991-06
Tuberous sclerosis
Tuberous Sclerosis Complex (International Child Neurology Association) by Paolo Curatolo, 2003-01-20
Genes on Chromosome 9: Tuberous Sclerosis
Tuberous sclerosis complex.(Clinical Snapshot): An article from: Dermatology Nursing by Laura Musse, 2005-10-01
Clinical and Genetic Investigations into Tuberous Sclerosis and Recklinghausen's Neurofibromatosis: Contribution to Elucidation of Interrelationship and Eugenics of the Syndromes. Acta Psychiatriaca et Neurologica Scandinavica Supplementum 71 by Allan Borberg, 1951-01-01
Clinical and Genetic Investigations into Tuberous Sclerosis and Recklinghausen's Neurofibromatosis: Contribution to Elucidation of Interrelationship and Eugenics of the Syndromes. Acta Psychiatriaca et Neurologica Scandinavica Supplementum 71 by Allan Borberg, 1951-01-01
Tuberous Sclerosis in the Infant (Reprinted from the AMerican Journal of Diseases of Children October 1935, Vol. 50, pp. 954-965) by Joseph H. Globus, Herman Selinsky, 1935
Genodermatoses: Turner Syndrome, Joubert Syndrome, Neurofibromatosis, Von Hippel-lindau Disease, Tuberous Sclerosis, Freeman-Sheldon Syndrome
Tuberous Sclerosis - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers by Philip M. Parker, 2007-07-19

lists with details

Echocardiography
tuberous sclerosis. Echocardiography is routinely performed in patients with tuberous sclerosis to search for cardiac rhabdomyomas.
http://www2.umdnj.edu/~shindler/tuberous_sclerosis.html

Extractions: E-chocardiography Journal: Alphabetical List Chronological List Images Home Page Echocardiography is routinely performed in patients with tuberous sclerosis to search for cardiac rhabdomyomas. Clinical description at the Online Mendelian Inheritance in Man OMIM database. Adenoma sebaceum. Rhabdomyoma of the heart: pathological specimen. This image is located on the Web Path Internet Pathology Laboratory for Medical Education at the University of Utah. 1. Nir A, Tajik AJ, Freeman WK, Seward JB, Offord KP, Edwards WD, Mair D, Gomez MR. Tuberous sclerosis and cardiac rhabdomyoma. Am J Cardiol 1995 Aug 15;76(5):419-21 Echocardiographically detected cardiac rhabdomyomata were common in patients with tuberous sclerosis. They were more prevalent and prominent in the younger patient. Tumors regress in size or number, or both, in most patients aged less than 4 years, and less so in older patients. 2. Muhler EG, Turniski-Harder V, Engelhardt W, von Bernuth G. Cardiac involvement in tuberous sclerosis. Br Heart J 1994 Dec;72(6):584-90
Tuberous Sclerosis. DermNet NZ
tuberous sclerosis information for patients. NZ DermNet is an online dermatology resource for patients, GPs and dermatologists. tuberous sclerosis.
http://www.dermnetnz.org/dna.genodermatosis/tubscler.html

Extractions: Home Systemic Tuberous sclerosis (TS) or tuberous sclerosis complex (TSC) is a genetic disorder that is characterised by hamartomas in many organs, but particularly the skin, brain, eye, kidney and heart. Hamartomas are non-cancerous malformations composed of overgrowth of the cells and tissues that normally occur in the affected area and include naevi (birthmarks). Skin lesions, epileptic seizures and developmental delay/behavioural problems are the main features of TSC. However, individuals with the condition may be affected in many different ways and with differing degrees of severity. Some patients may have very few or no symptoms at all, whilst others may be severely affected with a multitude of symptoms. Tuberous sclerosis is a genetic disorder. About one third of all cases of TS are inherited from an affected parent. All other cases are due to sporadic new mutations of the tuberin protein gene occurring in the early stages of life. People of all races and sex may be affected. The condition may become apparent any time from infancy to adulthood but usually occurs between 2-6 years of age.
Tuberous Sclerosis
tuberous sclerosis Bourneville s Disease - Epiloia. We report a case of renal cell carcinoma of the right kidney associated with tuberous sclerosis .
http://www.edae.gr/tuberous.html

Extractions: Bourneville's Disease - Epiloia A case of renal cell carcinoma associated with tuberous sclerosis Kakimoto K; Mori N; Tei N; Hara T; Koide T . Tuberous sclerosis is associated commonly with renal angiomyolipoma. On the other hand, the relation between tuberous sclerosis and renal cell carcinoma is not widely recognized. We report a case of renal cell carcinoma of the right kidney associated with tuberous sclerosis.... Tuberous Sclerosis - October 1999 A.S.T. Associazione Sclerosi Tuberosa American Brain Tumor Association Homepage American Society of Human Genetics Ash-Leaf Spots in Tuberous Sclerosis The New England Journal of Medicine June 25, 1998 Vol. 338, No. 26 Australasian Tuberous Sclerosis Association Australasian Tuberous Sclerosis Society Inc. (ATSS) The Australasian Tuberous Sclerosis Society Inc. (ATSS) was foundered in 1982, with a mission statement: "ATSS aims to support Tuberous Sclerosis families, educate an inform health professionals and the community." ATSS acts as a mutual support group for sufferers, relatives and health professionals, sharing problems and information by providing: Australasian Tuberous Sclerosis Society ATSS Autism Research Institute Autism Society of America Basic facts about Tuberous Sclerosis..
Uhrad.com - Neuroradiology Imaging Teaching Files
uhrad.com Neuroradiology Imaging Teaching Files. Case Thirty Nine - tuberous sclerosis. Diagnosis tuberous sclerosis. Discussion
http://www.uhrad.com/mriarc/mri039.htm

Extractions: Click on Images for Enlarged View Clinical History: None given. Findings: Image #1 is an axial (T1 weighted scan demonstrating multiple cystic appearing lesions within the white matter. In addition, there is a small subependymal nodule within the anterior horn of the right lateral ventricle. Image #2 demonstrates a region of decreased signal intensity located within the left frontal cortex consistent with a cortical tuber. In addition, subependymal nodules are identified within the lateral ventricles. Image #3 demonstrates enhancement of a right lateral ventricle subependymal nodule. Diagnosis: Tuberous sclerosis. Discussion: References:
Encyclopaedia Topic : Tuberous Sclerosis, Section : Introduction
tuberous sclerosis. Search. Help. Introduction. tuberous sclerosis (TS) is a genetic disorder. It is sometimes refered to as tuberous sclerosis Complex (TSC).
http://www.nhsdirect.nhs.uk/en.asp?TopicID=650
Tuberous Sclerosis
tuberous sclerosis Complex. What is it? tuberous sclerosis is a genetic disorder which results in tumor formation in many parts of the body.
http://rarediseases.about.com/cs/tuberoussclerosis/a/051703.htm

Extractions: zJs=10 zJs=11 zJs=12 zJs=13 zc(5,'jsc',zJs,9999999,'') About Rare / Orphan Diseases Rare Diseases S - V Rare Diseases: T ... Rare cancers zau(256,152,145,'gob','http://z.about.com/5/ad/go.htm?gs='+gs,''); Is it a Rare Disease? Rare Diseases A - B Rare Diseases C - D Rare Diseases E - H ... Help zau(256,138,125,'el','http://z.about.com/0/ip/417/0.htm','');w(xb+xb); Subscribe to the About Rare / Orphan Diseases newsletter. zau(256,152,100,'hs','http://z.about.com/5/ad/hs.htm?zIhsid=00',''); Search Rare / Orphan Diseases Email to a friend Print this page Stay Current Subscribe to the About Rare / Orphan Diseases newsletter. Suggested Reading Internet links on tuberous sclerosis Elsewhere on the Web Information pamphlet: tuberous sclerosis Tuberous Sclerosis Alliance Most Popular ALD and Lorenzo's Oil The Elephant Man's Bones Reveal Mystery Prune Belly (Eagle-Barrett) Syndrome Progeria Syndromes ... Mad Cow Disease and Humans What's Hot Autoimmune Kidney Disease Tourette Syndrome Christmas Disease Bugs, PANDAS, and Tics ... Dystonia and Botox Injections From Mary Kugler
DermIS / Main Menu / DOIA / Alphabetically / Diagnosenames Containing 'tuberous
DermIS / main menu / DOIA / alphabetically / diagnosenames containing tuberous sclerosis , deutsch español portugues français. tuberous sclerosis, 12.
http://www.dermis.net/doia/abrowser.asp?zugr=d&lang=e&beginswith=tuberous sclero
Tuberous Sclerosis - Eurorad - Clinical Case 943 - Resident
teaching files,radiology,tuberous sclerosis,with mental retardation, seizures and multiple facial Pringle fibroadenomas was admitted for respiratory distress
http://www.eurorad.org/case.cfm?uid=943
Diffusion MRI In Tuberous Sclerosis - Eurorad - Clinical Case 646 - Resident
teaching files,radiology,Diffusion MRI in tuberous sclerosis,Facial angiofibroma, seizures, and developmental delay.,tuberous sclerosis,EAR,ECR,elearning,e
http://www.eurorad.org/case.cfm?uid=646
Tuberous Sclerosis
Links to information about tuberous sclerosis. Created May 2004. 5 Resources Found There is no cure. Nov 2002; tuberous sclerosis what causes it?
http://www.healthinsite.gov.au/topics/Tuberous_Sclerosis
Tuberous Sclerosis
tuberous sclerosis,. Print this article, The diagnostic criteria for the tuberous sclerosis complex include a number of primary, secondary and tertiary features.
http://www.amershamhealth.com/medcyclopaedia/medical/Volume VII/TUBEROUS SCLEROS

Extractions: Amershamhealth.com Search for: Type a word or a phrase. All forms of the word are searchable. Browse entry words starting with: A B C D ... Other characters Tuberous sclerosis, a phakomatosis which is inherited in an autosomal dominant fashion and affects multiple organ systems. Classically it is characterized by a clinical triad of epilepsy, mental retardation and skin lesions (adenoma sebaceum). The diagnostic criteria for the tuberous sclerosis complex include a number of primary, secondary and tertiary features. In a large proportion of patients, infantile spasms or myoclonic seizures in early childhood are the presenting features. Approximately 10% of children with infantile spasms will have tuberous sclerosis. Radiology, and in particular neuroimaging, plays an important role in the diagnosis of tuberous sclerosis, with characteristic abnormalities appearing on neuroimaging in more than 95% of patients. Intracranial manifestations The intracranial manifestations can be divided into a number of major areas: subependymal hamartomas, giant cell tumours, cerebral hamartomas, white matter lesions, parenchymal cysts, cerebellar lesions and avascular lesions. Subependymal hamartomas The subependymal hamartomas appear as nodules of tissue along the walls of the ventricular system, most commonly the lateral ventricles. The imaging appearances change with the age of the child. In the first year or two of life they are rarely calcified and thus difficult to detect on CT, but later they are clearly visualized (
Tuberous Sclerosis
tuberous sclerosis,. Print this article, tuberous sclerosis, Fig. 1. a. CT scan without contrast. Bilateral hyperdense calcifications in subependymal hamartomas.
http://www.amershamhealth.com/medcyclopaedia/medical/Volume VI 1/TUBEROUS SCLERO

Extractions: Amershamhealth.com Search for: Type a word or a phrase. All forms of the word are searchable. Browse entry words starting with: A B C D ... Other characters Tuberous sclerosis, (TBS), (also called Bourneville Pringle disease), autosomal dominant disorder with variable expressivity and genetic heterogeneity (two loci are recognized: one on 9q34 and one on 16p13). The incidence is reported as between 1/10,000 and 1/150,000 births with no sexual predilection. Other frequent lesions are cardiac rhabdomyoma (80% of cardiac rhabdomyomas are associated with tuberous sclerosis), intra- and extracranial aneurysms, renal angiomyolipomas, carcinomas, pulmonary lymphangiomyomatosis, cysts, interstitial reticular infiltrates and spontaneous pneumothorax. Various skeletal and endocrine manifestations can be present. The four major intracranial manifestations of TBS are cortical tubers, white matter abnormalities, subependymal nodules and subependymal giant cell astrocytoma. All these lesions are postulated to represent the same defect of cell proliferation and differentiation in the germinal matrix with resulting disorders of migration and cortical organization, variably expressed all along the glioneuronal units. Cortical tubers are the most characteristic and epileptogenic lesions of TBS. They are nodules that involve both the cortex and the underlying white matter, composed of bizarre giant astrocytic and neuronal cells, dense fibrillary gliosis and diminished, disordered myelin sheaths. As the pathological findings in cortical tuber are similar to those of focal cortical dysplasia (FCD) with balloon cells (BC), some authors believe that FCD with BC and formes frustes of TBS may in fact represent the same entity.
Tuberous Sclerosis
BioethicsWeb MedHist pscicom. SEARCH BROWSE ABOUT WHAT S NEW SUBMIT SITE TRAINING SITE MAP, tuberous sclerosis. tuberous sclerosis Association (TSA).
http://omni.ac.uk/browse/mesh/C0041341L0041341.html

Extractions: low graphics other: Ataxia Telangiectasia Canavan Disease Cockayne Syndrome Hepatolenticular Degeneration ... Tuberous Sclerosis Association (TSA) The Tuberous Sclerosis Association (TSA) was formed in 1977 to offer support to patients and families.The site provides general information about the charity, including activities, fundraising, research projects and publications. There is also information about Tuberous Sclerosis which is updated regularly. Tuberous Sclerosis Great Britain Charities
AllRefer Health - Tuberous Sclerosis: Calling Your Health Care Provider (Adenoma
tuberous sclerosis (Adenoma Sebaceum) information center covers Calling Your Health Care Provider. Provider. tuberous sclerosis.
http://health.allrefer.com/health/tuberous-sclerosis-doctor.html

Extractions: AllRefer Channels :: Yellow Pages Reference Health Home ... Contact Us Quick Jump ADD/ADHD Allergies Alzheimer's Disease Arthritis Asthma Back Pain Breast Cancer Cancer Colon Cancer Depression Diabetes Gallbladder Disease Heart Attack Hepatitis High Cholesterol HIV/AIDS Hypertension Lung Cancer Menopause Migraines/Headaches Osteoporosis Pneumonia Prostate Cancer SARS Stroke Urinary Tract Infection 1600+ More Conditions Alternative Medicine Health News Symptoms Guide Special Topics ... Medical Encyclopedia Go To Main Page Alternate Names : Adenoma Sebaceum Calling Your Health Care Provider Notify your health care provider if either side of the family has a history of tuberous sclerosis. Since tuberous sclerosis also appears as a spontaneous mutation, call your health care provider if you notice symptoms suggestive of tuberous sclerosis in your child. Call a geneticist if your child is diagnosed with cardiac rhabdomyoma, as tuberous sclerosis is the leading cause of this tumor.
AllRefer Health - Tuberous Sclerosis (Adenoma Sebaceum)
tuberous sclerosis (Adenoma Sebaceum) information center covers causes, prevention, symptoms, diagnosis, treatment, incidence, risk factors, signs, tests
http://health.allrefer.com/health/tuberous-sclerosis-info.html

Extractions: AllRefer Channels :: Yellow Pages Reference Health Home ... Contact Us Quick Jump ADD/ADHD Allergies Alzheimer's Disease Arthritis Asthma Back Pain Breast Cancer Cancer Colon Cancer Depression Diabetes Gallbladder Disease Heart Attack Hepatitis High Cholesterol HIV/AIDS Hypertension Lung Cancer Menopause Migraines/Headaches Osteoporosis Pneumonia Prostate Cancer SARS Stroke Urinary Tract Infection 1600+ More Conditions Alternative Medicine Health News Symptoms Guide Special Topics ... Medical Encyclopedia Go To Main Page Alternate Names : Adenoma Sebaceum Definition Tuberous sclerosis is a group of two genetic disorders characterized by problems with the skin, brain/nervous system, and kidneys, and a predisposition to tumors. The diseases are named after a characteristic abnormal growth in the brain, which takes the shape of a tuber or root. Tuberous Sclerosis, Hypopigmented Macule Tuberous sclerosis is inherited as an autosomal dominant trait (only one parent must pass on the bad gene for the child to get the disease). However, a high percentage of cases are due to new mutations (which occur in the sperm or egg of one of the parents that created the particular child), so there usually is no family history of the disease.
Special Child: Disorder Zone Archives - Tuberous Sclerosis
tuberous sclerosis. The name, tuberous sclerosis, comes from tuberlike growths in the brain which calcify with age and become hard, or sclerotic.
http://www.specialchild.com/archives/dz-022.html

Extractions: Matthew Carlos Introduction Tuberous sclerosis (TSC) is a rare genetic disorder that is characterized by benign tumors in vital organs such as the brain, eyes, kidneys, heart and skin. The name, tuberous sclerosis, comes from tuber-like growths in the brain which calcify with age and become hard, or sclerotic. The condition develops before birth, occurs in both males and females, and is seen in all races and ethnic groups. There are 25,000 to 40,000 individuals in the United States with TSC and approximately 1,000,000 worldwide. TSC has an occurrence rate of 1 out of 5,800 live births, although it is believed that there are many undiagnosed cases. TSC is caused by two different defective genes; a defective gene on chromosome 9q34 called TSC1 and a defective gene on chromosome 16p13 called TSC2. Only one of these two genes needs to be affected for the individual to have TSC. One-third of the cases of TSC are hereditary and are autosomal dominant, meaning that only one parent needs to have the defective gene to pass it on to the child. In this case, each child has a 50% chance of inheriting TSC. The other two-thirds are the result of a spontaneous (or new) mutation. A case of TSC was first described by Von Recklinghausen in 1862. In 1880, Bourneville gave a complete description and name to the disorder.
TheFetus.net - Tuberous Sclerosis -Philippe Jeanty, MD, PhD & Sandra R Silva, MD
net. tuberous sclerosis. Updated 8/13/2003 by Pedroli Gianluca MD. Figure 1 The typical café au lait spot of tuberous sclerosis. Synonyms
http://www.thefetus.net/page.php?id=445
TheFetus.net - Tuberous Sclerosis-Luc Gourand, MD
200308-14-12 tuberous sclerosis © Gourand www.TheFetus.net. tuberous sclerosis. Luc Gourand, MD. Service De Médecine Foetale, Institut
http://www.thefetus.net/page.php?id=1303
Clinical Neurogenetics, Wake Forest
tuberous sclerosis and Subependymal Giant Cell Astrocytoma. NTSA s National tuberous sclerosis Association Homepage Connecticut tuberous sclerosis Association.
http://www.wfubmc.edu/surg-sci/ns/ngenet.html

Extractions: An International Listing of VHL Support Organizations Information in French Information in Spanish Information in German The Danish VHL Association Danish and English von Hippel-Lindau Disease from the National Institute of Neurological Disorders and Stroke (USA) What is von Hippel-Lindau Disease? Is there any treatment? What is the prognosis? What research is being done? ... Stereotactic Radiosurgery for Hemangioblastomas of the Brain. Ajay Jawahar, M.S., Douglas Kondziolka, M.D., Yolanda I. Garces, M.D., John C. Flickinger, M.D., Bruce E. Pollock, M.D., and L. Dade Lunsford, M.D. UPMC Presbyterian, Pittsburgh, PA. National Cancer Institute Kidney Cancer Web Page Galaxy.Net's
Tuberous Sclerosis
tuberous sclerosis. Overview Treatment. Definition. Causes, incidence, and risk factors. tuberous sclerosis is inherited as an autosomal dominant trait.
http://www.npi.ucla.edu/PEDSNEUROPSYCH/Tuberous_Sclerosis/body_tuberous_sclerosi

Extractions: Tuberous Sclerosis Treatment Definition An inheritable disorder characterized by skin lesions , varying degrees of mental retardation , and seizures Causes, incidence, and risk factors Tuberous sclerosis is inherited as an autosomal dominant trait. It is one of a group of diseases described as neurocutaneous syndromes because of extensive involvement of both the skin and the central nervous system (brain and/or spinal cord). The symptoms of tuberous sclerosis, however, vary considerably from minimally affected people with normal intelligence and no seizures to severely affected people with profound retardation and frequent, difficult-to-control seizures. The disease is named after the typical brain lesion which is called a tuber. Severely affected people may develop seizures shortly after birth that are characterized by infantile spasms (hypsarrhythmia). Later seizures tend to be myoclonic. Mental retardation becomes evident as infants begin to miss their normal developmental milestones Several different skin lesions are common in tuberous sclerosis.

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