#Banana sign aeen in spina bifida
Cl bottulinum causes 
           food poisoning in canned food 
               food poisoning in infants due to honey 
floppy baby synd
remember NaCl for myotonia: 
1.Na--Paramyotonia congenita 
2.Cl--myo.congenita and gen.myotonia 
rem NaCa for periodic paralysis 
1.Na--Hyperkalemic 
2.Ca--Hypokalemic 
PoCa for Episodic ataxia 
K--type1 
Ca--type2 nd 6
Henoch scholein purpura 
mc leukocytoclastic vasculitis in children 
cf arthalgia purpura abdominal pain 
glycogen storage diaorder not seen im ms 
type i =von gierke disease g6pd def ms dont contain g6pd enzyme
Mc cune albright synd 
precious puberty multiple cystic bone lesions nerve deafness and endocrinopathies
Triad of Alports Syndrome 
Sensorineural deafness 
Progressive renal failure 
Ocular anomalies 
Triad of Behcet's Syndrome 
Recurrent oral ulcers 
Genital ulcers 
Iridocyclitis 
Beck’s Triad 
Muffled heart sound 
Distended neck veins 
Hypotension 
Charcot’s Triad 
Pain + fever + jaundice 
Gradenigos Triad 
Sixth cranial n. Palsy 
Persistent ear discharge 
Deep seated retro orbital pain 
Triad of Hypernephroma 
Pain + hematuria + renal mass 
Hutchinson’s Triad 
Hutchison's teeth 
Interstitial keratitis 
Nerve deafness 
Triad of Kwashiorkar 
Growth retardation 
Mental changes 
Edema 
Saint's Triad 
Gall stones 
Diverticulosis 
Hiatus hernia 
Trotter's Triad 
Conductive deafness 
Immobility of homolateral soft palate 
Trigeminal neuralgia
Whipple's triad 
symptoms consistent with hypoglycemia, a low plasma glucose concentration, relief of symptoms after the plasma glucose level is raised
Neuro blastoma 
mc malignancy in infancy 
origin =adrenals mediastinum neck 
presents as abd mass calcifications on xray proptosis sutural separation and multiple skeltal secondaries
Among the inhalational agents max rise in ICT is with enflurane followed by Halothane and minimum in Isoflurane
Immotile cilia synd kartagener syn 
              situs inversus bronchiestasis rhino sinusitis
opiods in spinal cord acts on substantia gelatinosa of dorsal horn cells
Colour synd 
Red baby vancomycin 
bronze baby phototherapy 
grey baby chloramphenicol 
blue eyes fair skin pku 
blue sclera path fractures osteogensis imperfect
Dyslexia learning disability 
alexithymia inability to recognise and describe feelings
Pseudoparalysois frog like position wimberger sign 
white line of frankel seen in scurvy
Mtp act 1971 
Transplantation act 1994 
Nrhm started 5/4/2005
SYNDROMES... 
• BROWN-SEQUARD SYNDROME: Damage(injury) to half of spinal cord ------> symptoms:Loss of pain and temperature sensation oncontra lateral side of body. Loss of proprioception and discriminatorytouch on ipsilateral side of body. 
CARDIO Syndrome`s• FLOPPY-VALVE SYNDROME: MitralIncompetence due to myxomatous degenerationof theleaflets.
• LERICHE'S SYNDROME: Occlusion of distalaorta ------>Hip, thigh, and calf fatigue.Impotence
• BEHCET'S SYNDROME: Vasculitis ------>secondary symptoms:Oral and genital ulcersUveitisOptic atrophy
• SHOULDER-HAND SYNDROME: Pain inshoulder and swelling in hand, sometimes occurringafter Myocardial Infarction.
• SICK SINUS SYNDROME: Chaotic atrial activity;continual changes in P-Waves. Bradycardia,alternating with recurrent ectopic beats and runs oftachycardia.
• SUPERIOR VENA CAVA SYNDROME: Causedby a tumor. Obstruction of SVC ------>EdemaEngorgement of the vessels of face,neck, and arms.Nonproductive coughDyspnea
• TAKAYASU'S SYNDROME: Arteritis of theAortic Arch, resulting in no pulse. Seen in youngwomen.
• WOLF-PARKINSON WHITE SYNDROME:ECG pattern of Paroxysmal Tachycardia.Short PR intervalDelta wave = early QRS complex.IATROGENIC (or Secondary to Medical Treatment)
• ASHERMAN'S SYNDROME: Adhesionswithin the endometrial cavity, causingamenorrhea and infertility.Adhesions probably were caused bysurgery.
• CARCINOID SYNDROME: Carcinoid tumorproducing Bradykinin Serotonin ------>secondary symptoms:Cyanotic flushingDiarrheaBronchial spasmEdema, ascites.
• GARDNER'S SYNDROME: Multipleinherited tumors, hereditary dominant trait.Skull osteomas, Fibromas,EpidermoidcystsColonic polyposis (APC gene) ------>predisposition to colonicadenocarcinoma.
• LAMBERT-EATON SYNDROME:Progressive proximal muscle weaknesssecondary to a carcinoma.
• MEIGS' SYNDROME: Fibroma of ovary withascites and hydrothorax
• PANCOAST SYNDROME: Tumor nearpulmonary apex ------>Neuritic pain of chest and armMuscle atrophy of the armHorner's Syndrome (impaired cervical
• PEUTZ-JEGHERS SYNDROME: Polyposis(hamartomas) of small intestineAlso see melanin pigmentation of buccalmucosa and skin around mouth and lips
Some CONGENITAL Syndromes-
• CERVICAL SYNDROME: Supernumerary C7 rib ------> Pressure on brachial plexus ------> painradiating over shoulder, arm, and forearm over C7distribution.
• DIGEORGE SYNDROME: Congenital absence of3rd and 4th Branchial Arches (Thymus and ParathyroidGlands) ------> secondary symptoms:No cell-mediated immunity ------> Frequentviral and fungal infectionsCharacteristic facial deformities
• DOWN SYNDROME: Trisomy 21. Mentalretardation, characteristic facial features, Simeoncrease in hand.
• FANCONI'S SYNDROME Type I: Bone-marrowhypoplasia ------> refractory anemia, pancytopenia.
• FETAL ALCOHOL SYNDROME: Fetalmalformations, growth deficiencies, craniofacialanomalies, limb defects.
• GOODPASTURE'S SYNDROME: Autoantibodiesagainst basement membranes ------>Glomerulonephritis (kidney) and hemoptysis (lungs).Often, death by renal failure
• KLINEFELTER'S SYNDROME:Trisomy XXY ------> testicular atrophy, increase in gonadotropins inurine.
• LESCH-NYHAN SYNDROME:Deficiency ofHGPRT (Hypoxanthine-Guanine Phosphoribosyltransferase------>Hyperuricemia, uric acid kidney stonesChoreoathetosisMental retardation, autism, spasticcerebral palsyX-Linked recessive
• MARFAN SYNDROME: Connective Tissuedisorder ------>Arachnodactyly: Abnormally longdigits and extremitiesSubluxation of lensDissecting aortic aneurism
• TURNER'S SYNDROME: XO monosomy.DwarfismWebbed neckValgus of elbow.Amenorrhea
• WILSON SYNDROME: Congenital defect inCeruloplasmin, leading to buildup of copper ------> mental retardation, cirrhosis, hepatolenticulardegeneration.
ENDOCRINE, REPRODUCTIVE Syndrome• CONN'S SYNDROME: PrimaryHyperaldosteronism ------> muscular weakness,hypertension, hypokalemia, alkalosis.
• CUSHING'S SYNDROME: Hypersecretion ofcortisol ------> secondary symptoms andcharacteristics:o Fatness of face and trunk.
 
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