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
Own Practice
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
Dental Surgeon
I.T.S CENTRE FOR DENTAL STUDIES AND RESEARCH
B.D.S


Radiologist
District Hospital
SN MEDICAL COLLEGE,
DMRD


North DMC Medical College & Hindu Rao Hospital
Radiologist
State Bank of India - Medical College Branch
DMRD

New Phc
Ayush Pharmashist
Kanpur Para Medical Institute
d.pharma

Trending Cases
What is the treatment of ulcer in angle of both lips again and again? I give tess oint there is recover but it produce again what is cause and treatment?
Dr. Nirmal Shah0 Like1 AnswerA female 36 years, gravida 3 para 2 comes with complaints of headache, loss of sight and is in labour with poor cervical dilatation progress. on admission, the BP is 178/102 with no history of convulsions and magnesium sulphate is given. A LSCS is performed under spinal anesthesia with BP stabilised. she is transferred to ICU for post operative management with BP continuing to increase . After 5 days, a feedback is given that the patient is discharged and gained her sight. What caused the loss of sight?
Dr. Prashant Vedwan1 Like0 Answer