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         Des Syndrome:     more books (58)
  1. Erbliche Polyposis-Syndrome des Magendarmtraktes: Genetische Untersuchungen zur Aufklärung der Heterogenität adenomatöser Polyposis-Syndrome (German Edition) by Stefan Aretz, 2010-08-27
  2. Le syndrome des Grieux: La relation pere/fils au XVIIIe siecle (French Edition) by Maurice Daumas, 1990
  3. Le syndrome des Plaines d'Abraham (French Edition) by Eric Schwimmer, 1995
  4. Maladie Du Système Nerveux: Autisme, Pathologie Neurologique Professionnelle, Autisme Infantile, Syndrome Des Jambes Sans Repos (French Edition)
  5. Syndrome: Syndrome D'épuisement Professionnel, Syndrome Métabolique, Syndrome Des Loges, Syndrome Myélodysplasique, Syndrome Du Savant (French Edition)
  6. Etude clinique et anatomo-pathologique des Syndromes Neuro-Anemiques, en particulier des Denegerescences combinees subaigues de la Moelle avec Anemie, avec 20 figures et une planche dans la texte (Travail de la Clinique des Maladies) by Dr. Pierre Mathieu, 1925
  7. La fievre des achats: Le syndrome des achats compulsifs (Collection Les empecheurs de penser en rond) (French Edition) by Jean Ades, 1999
  8. Syndrome Neurologique: Syndrome de Guillain-Barré, Syndrome D'enfermement, Syndrome Des Jambes Sans Repos, Syndrome Vestibulaire (French Edition)
  9. Appareil Locomoteur: Syndrome Des Loges, Kinésithérapie, Technique Bowen, Tendon, Rhumatologie, Traumatologie, Appareil Locomoteur Humain (French Edition)
  10. Gremoire : Tests Et éChelles De La Maladie D'alzheimer Et Des Syndromes Apparentés
  11. Neuroleptique: Alimémazine, Métopimazine, Dyskinésie Tardive, Syndrome Malin Des Neuroleptiques, Antidopaminergique (French Edition)
  12. Apiculture: Apiculteur, Apis, Hydromel, Syndrome D'effondrement Des Colonies D'abeilles, Miel, Prairie Fleurie, Élevage de Reines (French Edition)
  13. Médécine Vétérinaire: Plan de Crise Pour une Pandémie, Syndrome D'effondrement Des Colonies D'abeilles, Traces, Fièvre Aphteuse, Asticothérapie (French Edition)
  14. Nuisance Apicole: Syndrome D'effondrement Des Colonies D'abeilles, Vespa Velutina, Gaucho, Maladie Noire, Thiamethoxam, Philanthus Triangulum (French Edition)

101. KINDLER SYNDROME
An article and case study of this rare disease. Includes links.
http://digilander.libero.it/camdic/KINDLER.html
KINDLER SYNDROME
Prof. Camillo O. DI CICCO
Member of " DNA Repair Group " National Institutes of Health (NIH) Bethesda, Maryland.
VIth Congress of the European Society for Pediatric Dermatology (Abstract)
A case is reported of a 28 year old man referring the appearance of swollen blisters due to insignificant trauma since birth. Later he noticed progressive changes of the skin as teleangectasies, atrophic spots, sensivity to sun, dystrohic fingermails and webbing between fingers.
The patient was hospitalized several times for an appropriate diagnosis and asked for the permission to undergo an operation of plastic surgery in Paris to correct webbing of the hands.
The rare association of two congenital diseases, epidermolysis bullosa dystrophica and poikiloderma, leads to the diagnosis of a Kindler syndrome.
The Kindler Syndrome described by Theresa Kindler in 1954 is probably a variant of hereditary acrokeratotic Poikiloderma in whitch Poikiloderma is preceded by a tendency to blistering following traumatic blisters.
There are not many ultrastructural studies on this syndrome. The ultrastructural level of blister formation has not been well characterized. The cutis of the hand back of our patient has been examined at the electronic microscope and it shows a thinned epidermis with a normal keratinization and a compact corneous ortokeratosic layer. A dermo epidermic flaking is noticed in several points and at different levels.

102. Shaky-Leg Syndrome And Vitamin B(12) Deficiency
Correspondence about this condition to the New England Journal of Medicine.
http://www.nejm.org/content/2000/0342/0013/0981.asp

103. The Alexander Foundation - Funding And Research For Cloverleaf Syndrome
Alexander Foundation is a nonprofit charitable institution that supports the funding and research of Cloverleaf syndrome.
http://www.thealexanderfoundation.com/
var ns4class='' PO Box 1515
Arden, NC 28704

Home
Alex's Story
Our Purpose
How To Help
Contact Us
Events Cloverleaf Syndrome Kleeblattschadel Deformity, or cloverleaf syndrome is a type of craniosynostosis in which there is premature closure of multiple or all bones of the skull (sutures). This condition causes the head to form a cloverleaf shape. The head may be larger than normal due to accumulation of fluid (hydrocephalic) in the skull. The anomaly has been reported to carry dismal prognosis both in terms of neurological outcome as well as cosmetic appearance if treatment is delayed. Facial malformations include high forehead, severe proptosis, or exophthalmoses, beaked nose, and downward displacement of ears. Multiple breathing and feeding issues may occur.
"Most of the important things in the world have been accomplished by people who have kept on trying when there seemed to be no hope at all."
Dale Carnegie
See Alex's Story - "The Miracle Child" Foundation Info Alex Schon first inspired the foundation. His condition, many life challenges and indomitable spirit led to the foundation's goals.

104. BWH Renal Division Home Page
The Laboratory of Inherited Kidney Disease at the Harvard Medical School and Brigham and Women's Hospital is conducting research to identify genes involved in the development of focal segmental glomerulosclerosis and nephrotic syndrome.
http://www.brighamandwomens.org/patient/researchGroupDetails.asp?dept_id=38&

105. Uro-Néphrologie - Syndrome Néphrotique
syndromeparanéoplasique. Dernière modification de cette fiche 04/02/2001.
http://www.medinfos.com/principales/fichiers/pm-uro-syndnephro2.shtml

Voir tous les livres

SYNDROME NEPHROTIQUE
Diagnostic
Etiologique
Traitement, Conclusion

CIRCONSTANCES DE DECOUVERTE et DIAGNOSTIC positif 1) Signes fonctionnels C'est le une oligurie
2) Biologie a) Dans les urines
La Il n'y a aucun autre signe biologique urinaire, en particulier il n'y a pas d'
b) Dans le sang Le ionogramme La
Les troubles lipidiques consistent en une Une augmentation des facteurs II, V, VII, VIII et X VS
Enfin, l' 3) Par une complication Rarement inaugurales, elles sont de 3 types: complications thrombo-emboliques complications infectieuses , d'abord urinaires puis pulmonaires. + Les DIAGNOSTIC ETIOLOGIQUE anomalies immunologiques ASLO foyer infectieux Chez l' enfant . La ponction biopsie Chez l' adulte allergie Que ce soit chez l'enfant ou l'adulte, la hyalinose segmentaire et focale et la Elles sont responsables de - certaines polyarthrite cirrhose Viviali Webmaster : infos@medinfos.com

106. Mental Health
Information on insomnia, Restless Legs syndrome, sleep in the elderly, and nonmedicine countermeasures is provided by Medbroadcast, a Canadian health web-broadcaster.
http://www.medbroadcast.com/channel_section_details.asp?channel_id=1022&rela

107. Bernard-Soulier Syndrome Website And Registry
Information for physicians and patients to learn more about this syndrome.
http://www.bernard-soulier.org/
The GPIb-V-IX complex
Figure courtesy of Chris Ward MD, PhD You are visitor number:
Site last updated September 2003

108. July 1996 - SMJ: Antiphospholipid Syndrome...
Case study of a 32 year old woman who came to a hospital at 36 weeks pregnancy.
http://www.sma.org/smj/96jul20.htm
Antiphospholipid Syndrome
Associated With Seizures
Aaron Milstone, MD, Alexander Fan, and
Howard Fuchs, MD, Nashville, Tenn ABSTRACT:
Antiphospholipid antibodies have been associated with thrombosis, fetal wasting, and thrombocytopenia. We discuss a case of antiphospholipid syndrome with the rarely recognized presentation of generalized tonic-clonic seizure during pregnancy. This case emphasizes the need for evaluation of possible hypercoagulable states in young adults with cerebrovascular events or newly diagnosed seizures. Autoantibodies found in the antiphospholipid syndrome may have specificity for cardiolipin or interfere with in vitro coagulation. Anticardiolipin antibodies (aCLs) can be measured directly by quantitative assay; lupus anticoagulant (LA) must be detected indirectly by prolonged partial thromboplastin time (PTT), kaolin clotting time, or Russell's viper venom test (RVVT). Lupus anticoagulant and aCLs bind negatively charged or neutral phospholipids1; they have been found in patients with and without associated autoimmune disease, most notably with systemic lupus erythematosus.2 These polyclonal antibodies have become a subject of interest in the medical literature because their presence has been associated with increased risk of vascular occlusion. Antiphospholipid syndrome is commonly associated with arterial or venous thrombosis, cardiac valvular abnormalities, fetal wasting, thrombocytopenia, or cerebrovascular events.3 One report also proposed an association between the presence of LA and late-onset seizures.4 Our case shows a link between seizures, cerebral infarction, and LA.

109. InteliHealth: Premenstrual Syndrome (PMS)
What PMS is, its symptoms, what your doctor looks for, diagnosis, expected duration, prevention, treatment, when to call a professional, prognosis, and additional resources.
http://www.intelihealth.com/IH/ihtIH/EMIHC000/9339/23664.html
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Advertisement
Premenstrual Syndrome (PMS)
  • What Is It? Symptoms Diagnosis Expected Duration ... Additional Info
  • What Is It? Premenstrual syndrome (PMS) is a collection of physical, psychological and emotional symptoms that many women experience during the one to two weeks before a menstrual period. These symptoms disappear soon after the start of menstrual bleeding.

    110. NINDS Fahr's Syndrome Information Page
    Information sheet compiled by the National Institute of Neurological Disorders and Stroke.
    http://www.ninds.nih.gov/health_and_medical/disorders/fahrs.htm
    National Institute of Neurological Disorders and Stroke Accessible version Science for the Brain The nation's leading supporter of biomedical research on disorders of the brain and nervous system Browse all disorders Browse all health
    organizations
    More about
    Fahr's Syndrome
    Studies with patients Research literature Press releases
    Search NINDS... (help) Contact us My privacy NINDS is part of the
    National Institutes of

    Health
    NINDS Fahr's Syndrome Information Page
    Synonym(s):
    Familial Idiopathic Basal Ganglia Calcification
    Reviewed 05-06-2003 Get Web page suited for printing
    Email this to a friend or colleague

    Table of Contents (click to jump to sections) What is Fahr's Syndrome?
    Is there any treatment?
    What is the prognosis? What research is being done? ... Organizations What is Fahr's Syndrome? Fahr’s Syndrome is a rare, genetically dominant, inherited neurological disorder characterized by abnormal deposits of calcium in areas of the brain that control movement, including the basal ganglia and the cerebral cortex. Symptoms of the disorder may include deterioration of motor function, dementia, seizures, headache, dysarthria (poorly articulated speech)

    111. Klinefelter Syndrome Support Group Website
    Educational and support information about Klinefelter syndrome/XXY and its variants.
    http://klinefeltersyndrome.org
    Klinefelter Syndrome
    Support Group Home Page
    Living with Klinefelter Syndrome - My Story


    Send any comments or questions to the webmaster. Bookmark This Site To Return For Updates
    This page created by Stefan

    Read
    my Dreambook!
    Sign
    my Dreambook!
    The information, text, graphics, and links provided on this site are provided for those seeking information about Klinefelter Syndrome/XXY. The opinions of the webmaster are his alone and do not necessarily reflect the opinions of any organization with which he is affiliated. The webmaster does not warrant the accuracy, or completeness of any links provided herein. Submit your page to 34 popular sites for free, using one form! This page last updated on May 5, 2004. You are visitor since July 26, 2000

    112. Polycystic Ovary Syndrome
    What Is Polycystic Ovary syndrome? Jump to another section of this articlePolycystic Ovary syndrome What Are the Signs and Symptoms?
    http://kidshealth.org/teen/sexual_health/girls/pcos.html

    KidsHealth
    Teens Sexual Health For Girls
    Cecily never really worried that her periods weren't regular because, like many girls, she assumed her monthly cycle would take time to settle down. But then Cecily's periods stopped for several months, so she went to see her doctor. The doctor noticed that Cecily's acne had worsened and that she had gained a lot of weight since her last appointment. She said she wanted to check Cecily for a condition called polycystic (pronounced: pah-lee- sis -tik) ovary sydrome (PCOS) What Is Polycystic Ovary Syndrome?
    You can't see them, hear them, or feel them, but the hormones that regulate a girl's reproductive system make themselves known in many ways - they are responsible for her periods, breast development, and other aspects of becoming a woman. Both girls and guys produce hormones called androgens (pronounced: an -druh-junz), which play a role in sexual function. Although androgens are sometimes referred to as male hormones, every female produces them, too. In girls with PCOS, the ovaries produce higher than normal amounts of androgens, and this can interfere with egg development and release. Some of the eggs develop into

    113. XXY List Web Page
    A great support, bonding, and resource site for people with Klinefelter's syndrome.
    http://www.globalwebsol.com/xxy/
    Please Bookmark this Web Site! Welcome to the XXY list members home page!
    ** Friends..............You have become my PARACHUTE **
    Charles Plum, a U.S. Naval Academy graduate, was a jet fighter pilot in Vietnam. After 75 combat missions, his plane was destroyed by a surface-to-air missile. Plumb ejected and parachuted into enemy hands. He was captured and spent six years in a Communist prison. He survived that ordeal and now lectures about lessons learned from that experience. One day, when Plumb and his wife were sitting in a restaurant, a man at another table came up and said, "You're Plumb! You flew jet fighters in Vietnam from the aircraft carrier Kitty Hawk. You were shot down!" "How in the world did you know that?" asked Plumb. "I packed your parachute," the man replied. Plumb gasped in surprise and gratitude. The man pumped his hand and said, "I guess it worked!" Plumb assured him, "It sure did if your chute hadn't worked, I wouldn't be here today." Plumb couldn't sleep that night, thinking about that man. Plumb says, "I kept wondering what he might have looked like in a Navy uniform a Dixie cup hat, a bib in the back, and bell bottom trousers. I wondered how many times I might have passed him on the Kitty Hawk. I wondered how many times I might have seen him and not even said 'Good morning, how are you,' or anything because, you see, I was a fighter pilot and he was just a sailor."

    114. Syndrome Respiratoire Aigu Sévère (SRAS)
    Translate this page Santé Canada/Health Canada. Sauter toute navigation -touch directe z Sauterau menu vertical -touch directe x Sauter au menu principal -touch directe m,
    http://www.hc-sc.gc.ca/pphb-dgspsp/sars-sras/index_f.html
    www.sras.gc.ca
    Avis importants

    115. Tim's Turner Syndrome Page
    Some information about this disease and links to other sites.
    http://www.iland.net/~tdluke/trnrs.html
    This page uses frames, but your browser doesn't support them.

    116. Virtual Hospital: Tourette Syndrome
    A list of documents concerning Tourette syndrome and their relevant medical treatments as well as their related topics aimed at the public. Taken from the Iowa Health Book, a part of the University of Iowa's Virtual Hospital.
    http://www.vh.org/Patients/IHB/Psych/Tourette/HomePage.html
    Tourette Syndrome
    Editors: Gary R. Gaffney, M.D.
    Associate Professor
    Department of Psychiatry Becky Ottinger
    Joshua Child and Family Development Center
    Grandview, Missouri The University of Iowa Peer Review Status: Peer Reviewed by the Authors
    First Published: 1995
    Last Revised: May 2000 Table of Contents Definitions Physician/Treatment Information Academic/Student Information Other Internet Sites See related Patient Textbooks about Psychiatry See related Patient Topics Brain and Nervous System Genetics/Birth Defects Psychiatry or Tourette Syndrome See related Provider Textbooks about Psychiatry See related Provider Topics Brain and Nervous System Genetics/Birth Defects or Psychiatry Virtual Hospital Home Virtual Children's Hospital Home Site Map ... UI Health Care Home http://www.vh.org/adult/patient/psychiatry/tourettesyndrome/index.html

    117. Fibromyalgia
    News and articles, chat rooms, message boards, coping suggestions and events.
    http://www.immunesupport.com/

    Immune
    Support .com World's Largest Site! Over 5 million Annual Visitors Chat Rooms Message Boards Advisory Board "Tip of the Day" ...
    Getting a Soulful Workout: The Nia Technique Helps Those With Fibromyalgia Move With Meaning
    - An exercise discipline that rejects the credo of higher, faster, stronger in favor of having fun, setting your own pace and losing yourself in the moment was just what Sandy Feldstein was looking for after developing fibromyalgia. READ MORE
    New Technique Promises Faster Pain Relief from Fibromyalgia and More
    - Orthopedic pain emanating from bone and muscle is addressed in a variety of ways by a panorama of physicians, chiropractors, physical therapists and neuromuscular massage therapists. Now a physical therapist in California is training health professionals ... READ MORE
    Chronic Fatigue Syndrome Treatment: Neurocognitive Feedback
    - What looks like a video game actually helps Polly Little fight Chronic Fatigue Syndrome, a mysterious disease that debilitates both body and mind, "I wasn't even able to do simple things like giving a store clerk the right amount of change." READ MORE
    Fibromyalgia: The Answer Is Blowin' in the Wind
    - Dr. Kevin White quotes Bob Dylan in asking, "How many times can a man turn his head and pretend that he just doesn't see? These immortalized words have rung true repeatedly throughout the sordid history of humankind. Yet it should seem startling that ...

    118. SandDude On Gardner's Syndrome
    Patient's point of view on this condition (familial adenomatous polyposis), experiences with the condition and after colostomy, information, and related links.
    http://mywebpages.comcast.net/sanddude
    Introduction Gardner's syndrome is a disease that affects many parts of the body. The primary problems with Gardner's syndrome are in the digestive system Patients will have hundreds, sometimes thousands, of polyps throughout the large intestine more Support ... Caring and Sharing Yahoo! Groups - FAP/Gardner's syndrome
    Yahoo! Groups - Kids with Gardner's syndrome

    Yahoo! Groups - Desmoid tumour survivors

    The Desmoid Tumor Online Support Group
    ...
    FAP.org - FAP Support Group
    In a Nutshell SandDude's osteoma and the hairdresser
    SandDude's polyps

    SandDude's genetic mutation

    SandDude's ampulla of Vater
    ...
    What is a desmoid tumor?
    Surgery and More It was late June of 1988. I was 37 years old. Something didn't feel exactly right ... a little bit of pain, but nothing really that alarming. I told myself that I would go to the doctor if things were not any better after the July 4th weekend. And then ... more Food Food. I really love the food I use. After I lost my colon, I had a heck of a time figuring out what to eat. Some foods caused too much gas. Some foods ... more
    medterms.com

    119. DANDA - Developmental Adult Neuro-Diversity Association - Welcome
    Organisation for individuals with conditions such as Dyspraxia, Dyslexia, ADHD, and Asperger's syndrome.
    http://www.danda.org.uk
    Navigation

    Home
    About DANDA
    FAQs
    DANDA News ...
    Dyspraxia Manchester
    Welcome! You are Visitor:
    Search this site Search WWW Developmental Adult Neuro-Diversity Association Welcome to DANDA - Developmental Adult Neuro-Diversity Association, for people with conditions such as Dyspraxia, ADHD, and Asperger's Syndrome. A new organisation founded to better the lives of neuro-diverse people. DANDA's mission statement:
    "To see that adults with developmental neuro-diversity reach their full potential and play a full role in society" Enter your email address here to get sent updates of events and articles: The Objectives of DANDA are as follows:
    2) To raise awareness and understanding of these conditions in adulthood, particularly their assessment, their effects, their treatment and the inter-relationship between the different conditions 3) To establish networks of groups to help adults with these conditions get involved in activities for interaction, mutual support, and education, provided that the activities shall be charitable.

    120. Syndrome De Peters SNOF
    à rechercher dans la famille pour pouvoir fournir un conseil génétique
    http://www.snof.org/maladies/peters.html
    Accueil Annonces Art Histoire ... Homepage
    Syndrome de Peters
    Nous remercions les parents de la petite fille pour leur autorisation Rev 02-03-2003
    jmm
    Introduction
    Von Hippel en 1887, puis Peters en
    • absence de membrane de Descemet,
    Actuellement, le syndrome de Peters , et concernent la , l' iris , l' et le cristallin Ces maladies regroupent les syndromes de Peters Axenfeld et Le syndrome de Peters migration ou bien une dysfonction cerveau hypophyse , des cartilages , des os papilles dentaires
    Clinique
    On peut constater uniquement une amblyopie Une forme un peu plus grave associe des Plus grave encore est l'association d'une cataracte ou bien d'un contact le syndrome de Peters-plus Le syndrome de Kivlin-Krause
    et
    Traitement
    Il faut d'abord envisager un bilan glaucome En cas de cataracte , en sachant que cette chirurgie est toujours encourageants
    Bibliographie
    Beauchamp, G. R. : Anterior segment dysgenesis keratolenticular adhesion and aniridia. J. Pediat. Ophthal. Strabismus 17: 55-58, 1978. Cabral de Almeida, J. C.; Reis, D. F.; Llerena, J., Jr.; Neto, J. B.; Lopes Pontes, R.; Middleton, S.; Telles, L. F. : Short stature, brachydactyly, and Peters' anomaly (Peters'-plus syndrome): confirmation of autosomal recessive inheritance. J. Med. Genet. 28: 277-279, 1991

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