U
2025
The global attention deficit hyperactivity syndrome market is experiencing a significant growth, and will grow considerably in the next few years. Attention (ADHD) is a disorder in which ...
Report Code : A11269 | Category : Life Sciences
U
2025
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus (MPPH) syndrome is a rare disorder that affects the brain development. Affected individuals are born with megalencephaly (a large brain and head size). The brain and head ...
Report Code : A11443 | Category : Life Sciences
U
2025
Acute respiratory distress syndrome (ARDS) occurs when fluid builds up the elastic air sacs of lungs. These air sacs are known as alveoli. The build building up in ...
Report Code : A11445 | Category : Life Sciences
U
2025
Periodic fever syndrome is when a child has recurrent episodes of fever. It is a group of disorders and is a genetic condition. Each episode of fever is ...
Report Code : A11446 | Category : Life Sciences
U
2025
Usher syndrome is one of the many rare genetic disorders, and is primarily characterized by deafness. This deafness is noticed due to the impaired ability of the auditory ...
Report Code : A11447 | Category : Life Sciences
U
2025
Brugada syndrome is a genetic disorder in which the heart's electrical activity becomes abnormal. Therefore, it increases the risk of abnormal rhythm of heart and even sudden cardiac ...
Report Code : A11449 | Category : Life Sciences
U
2025
Dravet syndrome, earlier known as severe myoclonic epilepsy of infancy (SMEI), is an epilepsy syndrome that develops in infancy or early childhood. It can include a spectrum of ...
Report Code : A11450 | Category : Life Sciences
U
2025
Down syndrome occurs when a person has an extra chromosome. Chromosomes are small units of genes in the body. These chromosomes determine how the body of a baby ...
Report Code : A11549 | Category : Life Sciences
P
2021
The Asia-Pacific fertility services market size was valued at $4,529.06 million in 2020, and is expected to reach $20,492.95 million by 2030, registering a CAGR of 15.5% from 2021 to 2030.
Report Code : A13035 | Pages : 159 | Category : Life Sciences
U
2025
Fetal valproate syndrome may be developed in the babies if the mother or the baby is exposed to valproic acid during the early stages of pregnancy. Valproic acid ...
Report Code : A13321 | Category : Life Sciences
U
2025
Since inception of commercial and defense-related air travel, there has been constant increase in the number of people travelling internationally. In addition, globalization has fueled the idea of ...
Report Code : A13393 | Category : Life Sciences
U
2025
Marfan syndrome is a genetic disorder that affects connective tissue, specifically the fibers which connect and support the body organs. It affects the eyes, bones covering the spinal ...
Report Code : A13574 | Category : Life Sciences
U
2025
Report Overview The report covers exhaustive analysis of global Rett syndrome market in terms of qualitative and quantitative aspects. The report provides in-depth information on market size & forecast, current market trends, driving & res
Report Code : A13591 | Category : Life Sciences
U
2025
Malabsorption syndrome is a condition that prevents absorption of nutrients such as carbohydrates, fats, proteins, and vitamins through small intestine. It might be caused due to some damage in the small intestine from infection, medication, surgery, or disorders of some sorts.
Report Code : A14378 | Category : Life Sciences
U
2025
Sjogren’s syndrome is a progressive autoimmune disease, which is caused by chronic inflammation and the lymphocytic infiltration of exocrine glands.
Report Code : A14381 | Category : Life Sciences
U
2025
Chaple syndrome is also known as DAF or CD55 deficiency, which refers to a genetic disorder that is rare in nature related to the immune system. CHAPLE is ...
Report Code : A14417 | Category : Life Sciences
U
2025
Aicardi syndrome is a rare genetic disorder, the onset of which begins with involuntary muscle spasm between 4 months to 4 years of age, which, if recurrent, can be fatal at times.
Report Code : A14424 | Category : Life Sciences
U
2025
Blau syndrome is a monogenic disease that affects skin, eyes, and the joints. A single modification in one gene present in the body’s cell primarily causes this inflammatory disorder where the symptoms start in childhood, usually before the child is 4 years of age.
Report Code : A14425 | Category : Life Sciences
U
2025
Menkes syndrome is essentially a rare, X-linked genetic disorder of copper metabolism, which is caused by gene mutations of copper transporter ATP7A that disrupts the copper levels in the body and makes it hard for the body to properly distribute the copper throughout the body.
Report Code : A14445 | Category : Life Sciences
U
2025
Jarcho Levin Syndrome or Spondylocostal Dysostosis is a rare heritable axial skeleton growth disorder and is hence, a condition present by birth. It causes the malformation of vertebral bones, ribs.
Report Code : A14902 | Category : Life Sciences
U
2025
Duane syndrome, also known as Duane retraction syndrome (DRS), is a non-progressive congenital strabismus caused by faulty development of the 6th cranial nerve.
Report Code : A15371 | Category : Life Sciences
P
2024
The global genu recurvatum market was valued at $6.5 billion in 2023, and is projected to reach $11.2 billion by 2033, growing at a CAGR of 5.6% from 2024 to 2033.
Report Code : A324006 | Pages : 216 | Category : Life Sciences
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