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What is Asherman Syndrome | Clinical Presentation | Dr. Shonali Chandra
What is Asherman Syndrome | Clinical Presentation | Dr. Shonali Chandra administrator 1 Views • 2 years ago

Asherman Syndrome refers to synechiae formation inside the uterine cavity. This video provides an overview of the pathology, clinical presentation, diagnosis and treatment of Asherman Syndrome.

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The Medicine Decoded App is here! Link in the Description.
The content is provided in a crisp and concise manner for conceptual understanding and clinical orientation. It will cover the important and most often asked areas pertaining to undergraduate university exams and various postgraduate entrance exams.

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Poliposis Juvenil y Sindrome de Cowden. Polipos Colon
Poliposis Juvenil y Sindrome de Cowden. Polipos Colon administrator 4 Views • 2 years ago

Actualmente en Internado Médico
Ingenieras en Biotecnología a los 16 años
Step 1 USMLE, a los 20.
Rotación en Surgical Intensive Care Unit, Univ. de Miami.
Presidenta y Vicepresidenta del Mission:Brain UAM chapter
Cada una con más de 50 cirugías mayores de neurocirugía y ortopedia, como 1er. o 2do. ayudantes.
Dos trabajos en Congreso Latinoamericano de Neurocirugía
Miembros de la American Association of Neurological Surgeons
Las Polímatas más prolíficas en producciones de videos matemáticos, científicos y de medicina a nivel mundial.
Mission:Brain, organización no lucrativa, el Dr. Quiñones-Hinojosa (Director de Neurocirugía de la Clínica Mayo, campus Florida) y el Dr. Michael Lawton (Barrow Neurological Institute), como Presidente y Vice Presidente, para gastos neuroquirúrgicos en México y en el mundo.

Construyamos puentes juntos:

Donar a Mission:BRAIN: https://missionbrain.kindful.com/?campaign=1237665
Mission:brain:
https://www.missionbrain.org/

Activation of mTORC1 in hamartoma syndromes and spontaneous tumors
Activation of mTORC1 in hamartoma syndromes and spontaneous tumors administrator 2 Views • 2 years ago

Activation of mechanistic Target OF Rapamycin Complex 1 (mTORC1) in hamartoma syndromes and spontaneous tumors.

In tumor cells of patients with congenital hamartoma syndromes such as Cowden syndrome (CS), tuberous sclerosis complex (TSC) syndrome and Peutz-Jeghers syndrome, the phosphatidylinositol 3-kinase (PI3K) and the mammalian target of rapamycin complex 1 (mTORC1) are overactivated. Major reasons for their dysregulation are inactivating mutations in tumor suppressor genes that code for PTEN, TSC1/TSC2 or LKB1, which are negative regulators of PI3K/mTORC1 signaling.

#onkoview, #Cowdensyndrome, #tuberous sclerosis complex, #mutations, #tumor, #PTEN, #mTORC1, #PI3K, #rapamycin complex
Engaging with Rare Disease Communities and Patient Populations | Peter Stanich, MD
Engaging with Rare Disease Communities and Patient Populations | Peter Stanich, MD administrator 3 Views • 2 years ago

The Ohio State University Center for Clinical and Translational Science (CCTS) presented “Tools of the Trade: Rare Disease Research," a program designed to explain how rare disease research presents unique challenges and provide the information, tools, and resources available to help investigators successfully overcome these challenges.

Topics included:

• How to design a rare disease research study
• Recruiting and retaining study participants with rare diseases
• Connecting and partnering with rare disease community organizations
• Expert Reviewer Panel on getting grants funded, papers published, and results disseminated in rare disease research

Download the agenda: https://ccts.osu.edu/sites/def....ault/files/inline-fi

View all of the presentations from 'Tools of the Trade: Rare Disease Research' - May 10, 2016 ( https://www.youtube.com/watch?v=3VNIm8bmxUQ&list=PLkw6pa7n2OjUMJDWRkpyw4h-KbvtwzDwQ )

Visit The Ohio State University Center for Clinical and Translational Science's website ( https://ccts.osu.edu ) for more information on how researchers from The Ohio State University, The Ohio State Wexner Medical Center, and Nationwide Children's Hospital can get support for their clinical and translational research projects.

Learn more about the OSU CCTS's 'Tools of the Trade' workshop series and view more archived ToT workshops: https://ccts.osu.edu/content/tools-trade-archive

The Ohio State University Center for Clinical and Translational Science (CCTS) is supported by a Clinical and Translational Science Award (CTSA) from the National Center for Advancing Translational Sciences (NCATS), one of the 27 institutes and centers at the National Institutes of Health (NIH).

Learn more about the CTSA program on the NCATS website: https://ncats.nih.gov/index.php

Ehlers Danlos Syndrome in a Snap: 20 Second Mnemonic #shorts #medical #usmle
Ehlers Danlos Syndrome in a Snap: 20 Second Mnemonic #shorts #medical #usmle administrator 2 Views • 2 years ago

This video will help you to spot Ehlers Danlos quickly with an easy mnemonic.
Who Should Get Genetic Testing?
Who Should Get Genetic Testing? administrator 1 Views • 2 years ago

There are many factors that you need to know, which could merit testing your blood for a cancer predisposition gene.
Lhermitte-Duclos disease #Radiology Spotter Series-36 By Dr Sumer Sethi
Lhermitte-Duclos disease #Radiology Spotter Series-36 By Dr Sumer Sethi administrator 1 Views • 2 years ago

Lhermitte-Duclos disease Radiology Spotter Series-36 By Dr Sumer Sethi
Arzhela, mon histoire Syndrome de Cowden, cancer du rein
Arzhela, mon histoire Syndrome de Cowden, cancer du rein administrator 5 Views • 2 years ago

L'association Syndrome de Cowden a pour objectif de sensibiliser, d'informer, d'aider le public ainsi que les personnes et leurs proches atteintes par ce syndrome.
Le Syndrome de Cowden est une maladie génétique orpheline rare.
Le diagnostic est posé après une analyse génétique avec une prise de sang et la découverte d'une mutation du gène Pten.
Il est caractérisé par la présence d’hamartomes (tumeurs bénignes - non cancéreux) se formant sur et sous la peau, la poitrine, la thyroïde, le système gastro-intestinal, l'endomètre et le cerveau.
Mais également un risque accru de développer des tumeurs malignes (comme les cancers du sein, de l'endomètre, de la thyroïde, du rein).
On peut aussi trouver des problèmes de développement psychomoteur.
Un nombre important de familles est concerné par le spectre de trouble autistique.

Une fois le diagnostic posé un suivi est mis en place (écho mammaire, irm pelvien, dermatologue, irm des seins, écho des reins, écho de la thyroïde et coloscopie).
Un bon suivi permet de garder le syndrome sous contrôle et ainsi permettre une action rapide en cas de cancers.

Syndrome de Cowden (syndromecowden@gmail)
Meet Meghan Ortega: 'Inspirational Islander' of 2016
Meet Meghan Ortega: 'Inspirational Islander' of 2016 administrator 2 Views • 2 years ago

Teen survivor/activist's fight through Cowden's Syndrome has yet again won the hearts of Staten Islanders.
Differential Diagnosis of Overgrowth Conditions
Differential Diagnosis of Overgrowth Conditions administrator 3 Views • 2 years ago

Differential Diagnosis of Overgrowth Conditions
Matthew Warman, MD, Director, Orthopedic Research Laboratories Professor of Orthopedic Surgery Boston Children’s Hospital

The Rare Bone Disease TeleECHO Clinic Series is intended for medical professionals interested in treating patients with rare bone diseases. This recorded didactic presentation was part of a larger live session. To learn more about this program and register for upcoming sessions, go to https://oif.org/echo/rbd/.

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