Cleidocranial dysplasia
A rare autosomal dominant disorder caused by mutations in the RUNX2 gene. It is characterized by developmental abnormalities in the bones and teeth, including the complete or partial absence of the clavicles, delayed closure of the fontanels, protruding mandible, hypertelorism, scoliosis, and short stature.
Disease Alternative Name
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B.SC;BDS;PGDMLC;Cerficate Implantology
Govt Dental College Osmania
BDS
KGN Dental Trust
Dentist, Pharmacist
Al Badar Dental College and Hospital
B. D. S
SVIMS
MBBS Student
Sri Venkateswara Institute of Medical Sciences
MBBS
TANEJA DENTAL CLINIC & IMPLANT CENTRE
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I.T.S CENTRE FOR DENTAL STUDIES AND RESEARCH
B.D.S
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In your opinion which patient populations shown the most therapeutic response to structured meditation programs?
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A 50 yrs old patient (history given below) kindly suggest further management *Chief Complaints* Unresponsive/vomiting/headache/fever/seizure 2/left side weakness /episode/history of epitaxis 2 days back *History* K/c/o HTN with irregular medicine *Vitals* BP 210/120 Temp 103.f Pulse -122 Spo2 86% *Physical Examination* Left side weakness Patient is semiconscious but drowsy, moderately built, appears uncomfortable. In mild respiratory distress. Left-sided weakness noted. Vitals monitored. *Investigations* Attached *Diagnosis* Acute ischemic stroke with rt mca acute thrombosis *Management* Medical management Monocef/pantop/strocit/manitol/lobet infusion/nimodepin/Ecosprin gold/pcm/emeset/levera/deriphyllin/dexa/nebulizer/o2 inhaler
Dr. Manoj Kumar0 Like3 Answers
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