Fraxa
Human FMR1 wild-type allele is located in the vicinity of Xq27.3 and is approximately 39 kb in length. This allele, which encodes fragile X mental retardation protein 1, may play a role in the mediation of mRNA transport. Amplification of a trinucleotide repeat (CGG) within the gene is associated with fragile X syndrome.
Disease Alternative Name
Surendranagar Chc Hospital Chuda Under Ccras Npcdcs Programme
Research Associate
Shree O H NAZAR Ayurvedic College Surat
BAMS
Rani Sati Charitable
2 Years
BKHMC
BHMS
Kerala Institute of Medical Sciences
Professor and Senior Consultant Neurology
Medical College Thiruvananthapuram
MBBS,MD (Med) ,DM(Neurology),DNB(Neurology), FAAN(Fellow of American Academy of Neurology)
Ghazipur Government Homeopathic College & Hospital
Clinic
Ghazipur Government Homeopathic College & Hospital
B.H.M.S
DUMURGRAM G.P.
AYUSH MEDICAL OFFICER
METROPOLITAN HOMOEOPATHIC MEDICAL COLLEGE & HOSPITAL
B.H.M.S.
Mobile Medical Unit and Ambulance Service Providers
Medical Officer
Barkatullah University Institute of Technology
bhms
Baba Deep Singh Ji Hospital
Medical Supretendent Md
Staffordshire University London - Digital Institute
POST GRADUATION
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