Children's Health

Rickets

Rickets is a disease of caused by the deficient calcification of the bones in children leading to softening and weakening of the bones mainly due to the deficiency of vitamin D.
339 Views

School absence for children with infective diseases

Children with certain infectious diseases are usually advised to stay away from school both for the benefit of the child as well as to ensure that the infection is not transmitted from one child to the other.
175 Views

Rashes in infants

During the first few weeks of life, a baby's skin can exhibit a variety of rashes. Most of these are harmless and transient.
208 Views

Mantoux test

This is a diagnostic skin test for demonstration of the presence of hypersensitivity to tuberculosis, where a small amount of the tuberculin is injected under the arm skin and the reaction is interpreted
681 Views

Teenage problems

Teen-time is a mixed bag, there are hundreds of new aspects of life and living which are to be discovered in this period. Teens are often energetic, thoughtful, and idealistic, with a deep interest in what's fair and right. It is a phase when physical and psychological modulations are underway at a very rapid pace. The biggest advantage of this phase is that at this time one can modulate the mind and body as one wants, because the growth is still on; but it also means that any errors or neglect can lead to a permanent damage.
1813 Views

Protein Energy Malnutrition

Protein energy malnutrition (PEM) is a type of disease caused due to decreased intake of food and deficient protein in the food most commonly seen in children and to the debilitated and uncared.
1326 Views

Kallmann Syndrome

Kallmann syndrome rare inherited condition characterized by hypogonadism (decreased functioning of the glands that produce sex hormones), eunuchoidism and impaired or absent sense of smell.
456 Views

Adrenal Hyperplasia Congenital (General)

The term congenital adrenal hyperplasia encompasses a group of autosomal recessive disorders, each of which involves a deficiency of an enzyme involved in the synthesis of cortisol, aldosterone, or both and androgens (testosterone). Congenital adrenal hyperplasia is a family of genetic conditions affecting the adrenal glands. It can interfere with normal growth and development in children ? including normal development of the genitals.
789 Views

Acrodermatitis Enteropathica

Acrodermatitis enteropathica (AE) is an autosomal recessive disorder, metabolic disorder affecting the uptake of zinc, characterized by periorificial (around the natural orifices) and acral (in the limbs) dermatitis, alopecia (loss of hair), and diarrhea.
398 Views

Acid Ceramidase Deficiency

Acid ceramidase deficiency is a extremely rare autosomal recessive lysosomal storage disease that cause an accumulation of fatty material lipids leading to abnormalities in the joints, liver, throat, tissues and central nervous system.
402 Views

 

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