endocrine

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an instrument and some pictures with the caption that says cartotid body tumuur
Lyre Sign - Carotid body tumor 【 Most common age of Presentation - 40 to 50 years 】
Genetic disorders  Tay-Sachs disease Monogenic, autosomal recessive Central nervous system degrades, ultimately causing death. Most common among people of Jewish, ... People, Sickle Cell Anemia, Genetic Disorders, Nervous System, Central Nervous System, Chronic Disease, Disease, Disorders
tay-sachs disease - Google Search
Genetic disorders Tay-Sachs disease Monogenic, autosomal recessive Central nervous system degrades, ultimately causing death. Most common among people of Jewish, ...
August 3, 2013: Birt–Hogg–Dubé syndrome (BHD), also Hornstein–Birt–Hogg–Dubé syndrome, Hornstein–Knickenberg syndrome, and fibrofolliculomas with trichodiscomas and acrochordons is a human genetic disorder that involves susceptibility to kidney cancer, renal and pulmonary cysts, and noncancerous tumors of the hair follicles, called fibrofolliculomas. This disorder has been found in over 100 families worldwide, and is inherited in an autosomal dominant pattern. Genetic Diseases, Genetic Disorder, Kidney Cancer, Kidney Disease, Tumor, Tuberous Sclerosis, Medical
Birt–Hogg–Dubé syndrome - Wikipedia
August 3, 2013: Birt–Hogg–Dubé syndrome (BHD), also Hornstein–Birt–Hogg–Dubé syndrome, Hornstein–Knickenberg syndrome, and fibrofolliculomas with trichodiscomas and acrochordons is a human genetic disorder that involves susceptibility to kidney cancer, renal and pulmonary cysts, and noncancerous tumors of the hair follicles, called fibrofolliculomas. This disorder has been found in over 100 families worldwide, and is inherited in an autosomal dominant pattern.
a man with long hair and beard wearing a large headdress in the middle of a field
The Best Way To Travel With Wine in the UK - The Morning Star
Neurofibromatosis refers to a number of inherited conditions that are clinically and genetically distinct and carry a high risk of tumor formation. Neurofibromatosis is an autosomal dominant disorder, which means only one copy of the affected gene is needed for the disorder to develop. Which is why looking at family history's before pregnancy is VERY important for all people.
a diagram showing how to use the hypothhetic model of iron absorption regulation
The first paper describing TfR2 hemochromatosis identified two copies of the Y250X nonsense mutation in six patients from two unrelated Sicilian families. Further mutations have since been identified. Most of the patients who have been identified are Italians. However cases have been reported in French and Japanese patients. Hemochromatosis type 3 is considered a rare disorder.
an image of a child with broken leg and knee in different stages of development from birth to age
Spot Diagnosis
Achondroplasia, common cause of dwarfism. Occurs as a sporadic mutation in approximately 75% of cases (associated with advanced paternal age) or may be inherited as an autosomal dominant genetic disorder. Disorder itself is caused by a change in DNA for fibroblast growth factor receptor 3 (FGFR3), which causes an abnormality of cartilage formation. If both parents have achondroplasia, and both parents pass on mutant gene, it is very unlikely that homozygous child will live past a few months.
a little boy smiling and holding his hand up
Mandibulofacial Dysostosis (Treacher Collins Syndrome): Symptoms, Causes and Treatment
Mandibulofacial Dysostosis is a disorder characterized by deformities of the facial bones and skull. It is a rare type of syndrome which is inherited as an autosomal dominant disease.
an x - ray image of a hand with the fingers and hands extended to show bones
Polydactyly - Wikipedia
Polydactyly: extra fingers or toes. Polydactyly is associated with autosomal dominant mutations in single genes, i.e. it is not a multifactorial trait. But mutation in a variety of genes can give rise to polydactyly.
LEKARZKATOWICE: NEFRONOFTYZA (NPHP ang. NEPHRONOPHTISIS) Polycystic Kidney Disease, Polycystic Kidneys, Renal Disease, Renal, Pathology, Kidney, Adult
NEFRONOFTYZA (NPHP ang. NEPHRONOPHTISIS)
LEKARZKATOWICE: NEFRONOFTYZA (NPHP ang. NEPHRONOPHTISIS)
the words leopard geckos genetic 101 are displayed
Enigma Syndrome: Autosomal Dominant Disorder - Leopard Gecko Supplies & Care
enigma syndrome leopard geckos
CADASIL Information Page: National Institute of Neurological Disorders and Stroke (NINDS) Neurological Disorders, Mitochondrial, Neuropathy, Peripheral Neuropathy, Diabetic Neuropathy, Peripheral Nerve Injury, Genital Herpes, Tinnitus Symptoms
All Disorders | National Institute of Neurological Disorders and Stroke
CADASIL Information Page: National Institute of Neurological Disorders and Stroke (NINDS)
August 14, 2013: Cowden syndrome is a rare autosomal dominant inherited disorder characterized by multiple tumor-like growths called hamartomas and an increased risk of certain forms of cancer. Cowden syndrome is associated with loss-of-function mutations in PTEN, a tumor suppressor gene, leading to hyperactivity of the mTOR pathway. These mutations lead to characteristic features including macrocephaly, intestinal hamartomatous polyps, and benign skin tumors (multiple trichilemmomas.) Autoimmune Disease, Cowden
Cowden syndrome - Wikipedia
August 14, 2013: Cowden syndrome is a rare autosomal dominant inherited disorder characterized by multiple tumor-like growths called hamartomas and an increased risk of certain forms of cancer. Cowden syndrome is associated with loss-of-function mutations in PTEN, a tumor suppressor gene, leading to hyperactivity of the mTOR pathway. These mutations lead to characteristic features including macrocephaly, intestinal hamartomatous polyps, and benign skin tumors (multiple trichilemmomas.)
Fatal Familia Insomnia is an autosomal dominant inherited prion disease of the brain. This disease results in the complete loss of the ability to sleep. Only 28 families worldwide are known carriers of the FFI gene mutation and the initial mutation is believed to have originated out of Italy in 1765. There is a family in Italy, who are most affected by this disease, and are in the process of coming up with a cure. But as of today, there is no hope once the symptoms of FFI appear. Horror, Art, Don't Care, Insomnia Cures, Scary Eyes, Creepy, Scary, Inner Demons
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Fatal Familia Insomnia is an autosomal dominant inherited prion disease of the brain. This disease results in the complete loss of the ability to sleep. Only 28 families worldwide are known carriers of the FFI gene mutation and the initial mutation is believed to have originated out of Italy in 1765. There is a family in Italy, who are most affected by this disease, and are in the process of coming up with a cure. But as of today, there is no hope once the symptoms of FFI appear.
there are 3 types of gaucher disease . This is the type 2. Trigeminal Neuralgia, Failure To Thrive, Type, Thrive, Quick
there are 3 types of gaucher disease . This is the type 2.
a bottle of vrriv for injections sits in front of a white box
VPRIV (Velaglucerase Alfa for injection), by Shire Pharmaceuticals, Recalled due to Visible Particulate Matter – – AttorneyOne.com – Finding An Attorney Online, Just Got Easier
VPRIV (Velaglucerase Alfa for injection) a medicine used for long-term enzyme replacement therapy (ERT) in pediatric and adult patients with type 1 Gaucher disease., by Shire Pharmaceuticals, Recalled due to Visible Particulate Matter #RecalledProducts #GaucherDisease
the diagram shows changes in chromenoe and chromenone from normal to non - chromenone
Chronic Myelogenous Leukemia Treatment
Philadelphia chromosome; three-panel drawing shows a piece of chromosome 9 and a piece of chromosome 22 breaking off and trading places, creating a changed chromosome 22 called the Philadelphia chromosome. In the left panel, the drawing shows a normal chromosome 9 with the abl gene and a normal chromosome 22 with the bcr gene. In the center panel, the drawing shows chromosome 9 breaking apart in the abl gene and chromosome 22 breaking apart below the bcr gene. In the right panel, the drawing...
The Cornell-criterium has different values in men and women:  R in aVL and S in V3 >28 mm in men R in aVL and S in V3 >20 mm in women Nclex, Cardio, Stethoscopes, Medical Doctor, Medical Education, Cardiovascular System
Chamber Hypertrophy and Enlargment
The Cornell-criterium has different values in men and women: R in aVL and S in V3 >28 mm in men R in aVL and S in V3 >20 mm in women
an image of some pink and purple things in the water that is under microscope glass
WebPathology
Castleman's Disease : Hyaline-Vascular Type: Castleman’s disease (giant lymph node hyperplasia, angiofollicular lymph node hyperplasia, lymph node hamartoma) is a distinct form of lymph node hyperplasia. Hyaline-vascular type shows large lymphoid follicles scattered throughout the lymph node. Several sclerotic bands are also present. Hyaline-vascular type represents approximately 90% of cases of solitary form of Castleman’s disease. Remainder are plasma cell type.
an mri scan shows the area where two small pieces of brain are located
Maple syrup urine disease (MSUD) is a very rare metabolic disorder. It is an inborn error of amino acid metabolism, which classically affects the brain tissue resulting in impairment or death if untreated. DWI: the posterior limbs of the internal capsules and optic radiations and the central corticospinal tracts within the cerebral hemispheres exhibit diffusion restriction, which represents myelin splitting oedema. http://radiopaedia.org/articles/maple-syrup-urine-disease
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Inflammatory Bowel Disease- Crohn’s vs. Ulcerative Colitis
Diseased Skin - Lichen Planus Lichen planus is a fairly common, itchy, non-infectious type of rash that usually occurs in adults. Doctors use the word ‘lichen’ to mean small bumps on the skin. ‘Planus’ means ‘flat’, and tells us that the small itchy bumps that make up the rash of lichen planus have shiny flat tops Lichen Sclerosus, Acute Kidney Injury, Itchy Bumps, Types Of Rashes, Skin Rash, Autoimmune Disorder, Types Of Skin Rashes, Lichen Planus
Diseased Skin - Lichen Planus Lichen planus is a fairly common, itchy, non-infectious type of rash that usually occurs in adults. Doctors use the word ‘lichen’ to mean small bumps on the skin. ‘Planus’ means ‘flat’, and tells us that the small itchy bumps that make up the rash of lichen planus have shiny flat tops
Image of lungcancer Health, Salud, Types Of Cancers, Discover, Cravings, Stop Smoke, Mesothelioma, Medical News
Asbestos and Lung Cancer
Image of lungcancer
a close up of a human brain on a red background
Neuropathology
Huntington's disease = atrophy of caudate and putamen (loss of GABAergic neurons) -> chorea, psych changes (get CAGey), dementia; AD due to increased CAG repeats on 4p16.3 (vs. Friederich ataxia = GAA on 9p13! Fragile X = CGG on Xq27.3)
a diagram of the parts of an adult's neck, including tummy and lumba
GI Path Online
Benign Tumours and Tumour-Like Lesions of Stomach: Gastric Polyps
an animal's hair is seen in this image
Actinomyces bacterial infection- associated with IUD's
an image of the inside of someone's stomach, with small dots on it
Photo Storage
CADASIL = eosinophilic material in media -> lacunar infarct, NOTCH3 mutation on 19p, 45 yo F migraine with aura -> TIAs
Asteroid bodies - Google Search (in sarcoidosis) Crystals, Calcium, Cholesterol, Inclusion, Search, Google Search, Google, Body
Inclusions in granulomas:Schuamann (conchoidal) bodies, asteroid bodies, calcium oxalate crystals, Hamazaki-Wesenberg (H-W) bodies, cholesterol.
Asteroid bodies - Google Search (in sarcoidosis)
an image of purple and white cells
Homer Wright rosettes (circular grouping of dark tumor cells surrounding pale neurofibrils)--neuroblastoma, medulloblastoma, retinoblastoma
the structure of an animal's stomach is shown in purple
How would you manage a basal cell carcinoma? (Confirm diagnosis with biopsy and tumour excision with 3 mm clear margin. Other modalities o...
an image of the inside of someone's stomach, with red and white cells
Top 5 Membranous Glomerulonephritis Symptoms
Top 5 Membranous Glomerulonephritis Symptoms - http://www.healtharticles101.com/top-5-membranous-glomerulonephritis-symptoms/#more-8111
an image of the inside of someone's stomach
hsv encephalitis with cowdry body
an area that is very pink and purple with lots of white dots on it,
Desmoplastic medulloblastoma = patched gene. p53 = astrocytomas. EGRF = GBM and anaplastic astrocytomas. Neuroblastoma = n-myc. Oligo = LOH of 1p and 19q
an animal's stomach with multiple sections and small areas in the middle, including one section
Female Genital Pathology
ovary low grade serous ca = BRAF and KRAS, progresses from benign/borderline
the cells in this cell are purple and white
an image of the cells in purple and white
Wilms tumor = WT-1 gene on chromosome 11. WAGR syndrome (Wilms, aniridia, GU anomalies and retardation) encompasses PAX6. WT2 is with Beckwith-Wiedemann syndrome increase Wilms and hepatoblastoma. Use methylation assays for this.
Krabbe's/Globoid cell = galactosidase deficiency --> multinucleated histocytes, fatal by age 2 (Gaucher is GLUCOcerebrosidase deficiency) Insight, Parkinsons Disease, Conditioner, Rare, May
Neuropathology
Krabbe's/Globoid cell = galactosidase deficiency --> multinucleated histocytes, fatal by age 2 (Gaucher is GLUCOcerebrosidase deficiency)
"Henoch-Schonlein purpura (HSP) is an inflammation of the small blood vessels of the skin, joints, bowels and kidneys. When blood vessels get inflamed, they can bleed into the skin, causing a reddish-purple rash (purpura)." http://www.mayoclinic.org/diseases-conditions/henoch-schonlein-purpura/multimedia/henoch-schonlein-purpura/img-20006933 #RA #AutoImmune Blood Vessels, Rheumatoid Arthritis, Adrenals, Rheumatoid Arthritis Symptoms, Herbal Remedies
Henoch-Schonlein purpura
"Henoch-Schonlein purpura (HSP) is an inflammation of the small blood vessels of the skin, joints, bowels and kidneys. When blood vessels get inflamed, they can bleed into the skin, causing a reddish-purple rash (purpura)." http://www.mayoclinic.org/diseases-conditions/henoch-schonlein-purpura/multimedia/henoch-schonlein-purpura/img-20006933 #RA #AutoImmune
a notepad with the text distance meters on it
Download 6-Min Walk Test (trial) for Android
6 minute walk test | ... and everyone who administers the 6-minute walk test. Which is a less rigorous test used as an alternative method for evaluating exercise tolerance, although the gold standard for exercise tolerance is a graded cardiopulmonary exercise test.