Cerebral Autosomal Dominant Arteriopathy Health Feed

The joint hypermobility syndrome is a condition that features joints that easily move beyond the normal range expected for a particular joint. The joint hypermobility syndrome is considered a benign condition.
Your medical condition can be discussed in more detail over a video or audio call for further consultation.

If you are carrier or one copy of defective gene and your husband is also carrier or one copy of defective gene then your baby has chance of glutaric acidemia type 1.
if you husband is normal then baby will be normal

1. Avoid exposure to cold
2. Take bath with little warm water 3. Do steam inhalation regularly at least once a day
4. Warm salt water gargles daily 5 no cold water / cold drinks / ice creams and so on
6. No smoking/ avoid pollution 7. Wash hands after use of bath room and before and after eating food.
8 more warm liquids medicine can not be advised for open question for medicine contact on private consultation good luck.

It is autosomal dominant meaning 50 % of children have chance to get same.
Evidence shows that the syndrome is associated with an increased risk of extraintestinal malignancy, especially carcinomas of the pancreas, breast, and reproductive organs.

Congenital deformities of spine are different and muscular dystrophies are different. They are not same.

Delusional disorder refers to the condition in which an individual experiences non-bizarre delusions that are beliefs in things that aren't actually true. The delusions involve situations that take place in real life like being deceived or stalked, conspired against, etc but in actuality, these situations may be highly exaggerated or not true at all as they involve the misinterpretation of experiences or observations. This health problem tends to take place during the middle or later part of you...more

Meningomyelocele is the most severe type of spina bifida, a congenital defect that occurs when the backbone and spinal canal fail to close before the baby is born. It is a neural tube defect and is the most common disabling birth defect.
The exact causes of spina bifida are unknown but environmental and genetic factors are thought to play a role in its development.
A baby’s risk of developing the condition is higher if their mother is taking antiseizure medications, having folic acid def...more

Prenatal Diagnosis is the diagnosis of the fetus or unborn baby. By prenatal diagnosis, doctors examine the developing baby. There are two main methods for prenatal diagnosis, Chorionic Villus Sampling (CVS), and Amniocentesis. However, the prenatal diagnosis consists of several tests which help doctors to find out the genetic disorder of the fetus.

According to many studies, some parents are at higher risk of having a baby with a genetic problem or disorder. Due to this reason, it is a...more

Medical genetics is a branch of medicine that involves identifying the cause of human biological variation. Medical genetics help to determine the health and disease of a person which are hereditary in nature. It involves the study and counseling about the pathogenesis, etiology, and natural history of disorders and diseases that originate genetically.

Medical genetics is different from human genetics in the way that human genetics involves the research and scientific study of the genom...more

Endometriosis is a condition in which the endometrial cells lining the inside wall of the uterus begin to grow outside the uterus. In a majority of the cases, the growth is on the ovaries, the Fallopian tubes, or the tissues around the uterus. In rare cases, it occurs in other body parts. Normally, women in the age group of 30 to 40 years are prone to developing this condition and genetics is believed to be the reason behind this disorder. It is a serious medical condition if it causes discomfor...more