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NEET MDS Shorts

83440
Pedodontics

The type of load on teeth that is most destructive to the periodontium is horizontal.

55934
Radiology

Internal derangement of the TMJ can be best diagnosed by MRI.

87801
Dental Materials

Chelation of carboxyl groups of the polyacids with the calcium in the apatite of enamel and dentin is the main mechanism through which glass ionomer bonds to tooth structure.

Glass ionomers release fluoride which results in the inhibiton of the progression of secondary caries. GIC is relatively biocompatable.
They elicit a greater pulp reaction as compared to ZnoE but generally less compared to zinc phosphate cement.

30390
Periodontics

Gingival changes, specifically gingival enlargement (overgrowth), are known side effects associated with several classes of medications. Phenytoin (an anticonvulsant), cyclosporine (an immunosuppressant), and nifedipine (a calcium channel blocker) are the three major drugs widely recognized for causing this condition. 
Phenytoin induces gingival overgrowth in approximately 50% of patients.
Cyclosporine causes the condition in about 30% of patients.
Nifedipine and other calcium channel blockers have an incidence rate of around 10-20%.

17051
Biochemistry

The biochemical defect in Osteogenesis Imperfecta, type II is a deficiency in lysyl hydroxylase.

85647
Periodontics

Bone graft procedures are most successful in treating narrow three-wall defects.

58128
Radiology

Double intensifying screens with screen film significantly reduce exposure time by amplifying the X-ray effect. The screens convert X-ray photons to light photons, which expose the film more efficiently than direct X-ray exposure. This reduces radiation dose to the patient while maintaining image quality.

87165
NEETMDS

The appearance of the ulnar sesamoid bone is a reliable indicator of skeletal maturity and typically occurs at the onset of the pubertal growth spurt. This event is a key marker used in orthodontics and pediatrics to assess a child's developmental stage.

78587
General Medicine

Hemophilia A is an X-linked recessive disorder, caused by a deficiency of factor VIII. Since the patient's mother is a carrier, she must have one defective X chromosome and one normal X chromosome. The patient, being a male, has a 50% chance of inheriting the disorder from his mother, which is the most likely scenario given the family history and the X-linked inheritance pattern. Hemophilia B is also X-linked but would be mentioned as Christmas disease if it were the correct answer. Hageman trait is an autosomal recessive disorder related to factor XII, which is less common than Hemophilia A and B.

61531
General Medicine

The GBM is a critical component of the glomerular filtration barrier that normally prevents the passage of proteins into the urine. In the nephrotic syndrome, there are alterations in the GBM that lead to increased permeability and loss of proteins, particularly albumin, into the glomerular filtrate.

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