What syndrome causes stunted growth?

What syndrome causes stunted growth?

Hypopituitarism. Hypopituitarism can cause growth hormone deficiency which can lead to short stature. This condition is treated with growth hormone therapy.

What disorders affect growth and development?

This includes constant malnutrition, digestive tract diseases, kidney disease, heart disease, lung disease, diabetes, or chronic severe stress. Any of these conditions can cause growth problems. Endocrine (hormone) diseases. Growth can be affected by some conditions that disrupt hormones.

What disease is failure to grow in height?

GHD occurs in roughly 1 out of 7,000 births. The condition is also a symptom of several genetic diseases, including Prader-Willi syndrome. You may be concerned that your child isn’t meeting height and weight growth standards. But if it’s GHD, it’s important to know that it’s treatable.

What is growth syndrome?

Growth disorders are problems that prevent children from developing normal height, weight, sexual maturity or other features. Very slow or very fast growth can sometimes signal a gland problem or disease.

What is short stature syndrome?

Short stature is a general term used to describe a condition in which a child or a teen’s height is well below the average height of his or her peers.

What is Allen disease?

Allan-Herndon-Dudley syndrome is a rare disorder of brain development that causes moderate to severe intellectual disability and problems with movement. This condition, which occurs exclusively in males, disrupts development from before birth.

What is Allan-Herndon-Dudley syndrome?

Allan-Herndon-Dudley syndrome is a disorder of brain development that causes moderate to severe intellectual disability and problems with movement. This condition, which occurs exclusively in males, disrupts development from before birth.

Is Allan-Herndon-Dudley syndrome degenerative?

Background. Allan-Herndon-Dudley syndrome (AHDS) is an X-linked recessive neurodegenerative disorder caused by mutations in the SLC16A2 gene that encodes thyroid hormone transporter. AHDS has been rarely reported in China.

What is Allen’s disease?