DelveInsight’s Trending Reports 2022: Ehlers-Danlos Syndrome Market, X Linked Hypophosphatemia Market, Thyroid Eye Disease Market, Primoridal Dwarfism Market, Sialidosis Market.

Ehlers-Danlos Syndrome Market

Ehlers-Danlos syndrome (EDS) is a disease that weakens the connective tissues of your body. These are things like tendons and ligaments that hold parts of your body together. EDS can make your joints loose and your skin thin and easily bruised. It also can weaken blood vessels and organs.

Some facts of Ehlers-Danlos Syndrome Market Report are:

·         The combined prevalence of all types of Ehlers-Danlos syndrome appears to be at least 1 in 5,000 individuals worldwide.

·         Vascular EDS is reported to have a prevalence of 1 in 100,000 individuals, and cardiac-valvular EDS a prevalence of less than 1 in a million people.

·         The estimated prevalence for all EDS varies between 1/10,000 and 1/25,000, EDS type IV representing approximately 5 to 10% of cases.

View Report: https://www.delveinsight.com/report-store/ehlers-danlos-syndrome-market

Some of Ehlers-Danlos Syndrome Companies are:

·         Aventis Pharmaceuticals

·         EVAMED

·         Acer Pharma

·         And Many Others

View Report: https://www.delveinsight.com/report-store/ehlers-danlos-syndrome-market

Ehlers-Danlos Syndrome Therapies are:

·         Celiprolol

·         Irbesartan

·         And Many Others

 

X Linked Hypophosphatemia Market

X-linked hypophosphatemia is a hereditary renal phosphate-wasting disorder characterized by hypophosphatemia, rickets and/or osteomalacia, and diminished growth. Phosphate levels are low because phosphate is abnormally processed in the kidneys, which causes a loss of phosphate in the urine (phosphate wasting) and leads to soft, weak bones (rickets). XLH is usually diagnosed in childhood. Features include bowed or bent legs, short stature, bone pain, and severe dental pain. XLH is the most common form of hereditary hypophosphatemic rickets.

Some facts of X Linked Hypophosphatemia Market Report are:

·         According to study conducted by He ́le`ne et al., titled “Impaired quality of life in adults with X-linked hypophosphatemia and skeletal symptoms”, the estimated prevalence of X-linked hypophosphatemia was 4.8 per 100,000.

·         As per Endocrine Society, the Food and Drug Administration (FDA) estimates that XLH affects about 3,000 children and 12,000 adults in the United States

·         According to Phosphodiabetes E.V. Netzwerk Information Austausch, estimates that X-linked hypophosphatemia (XLH) is the most common form of vitamin D-resistant rickets and, with a prevalence of 4.8 cases per 100,000 individuals, is considered a rare disease.

·         The study by Riancho et al., titled “Osteomalacia and rickets” estimates that the prevalence of Hypophosphatemic rickets linked to the X chromosome due to a mutation in the PHEX gene is around 5 per 100,000.

View Report: https://www.delveinsight.com/report-store/x-linked-hypophosphatemia-market

Some of X Linked Hypophosphatemia Companies are:

·         Ultragenyx

·         Validus Pharmaceuticals

·         Prospec-Tany Technogene Ltd

·         Merck KGaA

·         Zeria Pharmaceutical Co., Ltd

·         Smith & Nephew

·         Narang Medical Limited

·         Eli Lilly and Company

·         F. Hoffmann-La Roche Ltd

·         And Many Others

View Report: https://www.delveinsight.com/report-store/x-linked-hypophosphatemia-market

X Linked Hypophosphatemia Therapies are:

·         Burosumab

·         Crysvita

·         And Many Others

 

Thyroid Eye Disease Market

Thyroid eye disease (TED)—also known as Graves’ Orbitopathy or Ophthalmopathy—is an autoimmune condition. It occurs when the body’s immune system attacks the tissue surrounding the eye causing inflammation in the tissues around and behind the eye. It appears that the same antibody that can cause thyroid dysfunction may also have an "attraction"to tissuessurrounding the eyes causing the onset of Graves' Ophthalmopathy. Moreover, the disease is categorized as mild, moderate, and severe.

Some of Thyroid eye disease Facts:

·         In a study by Zagaria et al. [2011], it was observed that approximately 25‐30% of patients with Graves’ disease have clinical evidence of Graves’ ophthalmopathy.

·         As per the study by Liaboe et al., titled “An Introductory Tutorial and Overview of Disease”, TED has a higher prevalence in women than men (16 per 100,000 vs. 3 per 100,000, respectively). Both men and women demonstrate a bimodal pattern of age of diagnosis(40–44 and 60–64 yearsin women; 45–49 and 65–69 years in men).

·         The study by Lazarus et al. titled “Epidemiology of Graves’ orbitopathy (GO and relationship with thyroid disease” estimates that Graves’ ophthalmopathy (GO) occurs mainly, but not exclusively, in patients with Graves’ disease. However, only about <50% of Graves’ patients have clinically apparent ophthalmopathy, where the approximate prevalence is 0.25%.

·         According to a review article titled “Epidemiology and Prevention of Graves’ Ophthalmopathy” by Wilmar et al., Graves’ ophthalmopathy is clinically relevant in approximately 50% of patients with Graves' disease, and severe forms affects less than 5% of patients.

View Report: https://www.delveinsight.com/report-store/thyroid-eye-disease-market

Some of Thyroid eye disease Companies:

·         Immunovant Sciences

·         Horizon Therapeutics

·         And Many Others

Thyroid eye disease Drugs Covered:

·         IMVT‐1401

·         Teprotumumab

·         And Many Others

View Report: https://www.delveinsight.com/report-store/thyroid-eye-disease-market

 

Primoridal Dwarfism Market

Primordial dwarfism is a rare and often dangerous group of genetic conditions that result in a small body size and other growth abnormalities. Signs of the condition first appear in the fetal stage and continue through childhood, adolescence, and adulthood.

Some facts of Primordial Dwarfism Market Report:

·         Primordial Dwarfism Market size is expected to change for 7MM during the forecast period of 2018-30.

·         Its prevalence report estimates 4 million babies to die in the first 4 weeks of life (the neonatal period) with almost 99 % of neonatal deaths (Lawn et al. 2011; Cous-ens et al. 1995).

·         The modern prevalence of MOPDII is unknown, but between 150 and 200 cases are reported worldwide each year (Bober and Jackson, 2017).

·         All types of primordial dwarfism are caused by changes in genes. Different gene mutations cause the different conditions that make up primordial dwarfism.

·         Primordial dwarfism can be difficult to diagnose. This is because the small size and low body weight could be a sign of other things, such as poor nutrition or a metabolic disorder.

To get more detailed insight on Primordial Dwarfism Market Report @Request for a Sample Report here: https://www.delveinsight.com/report-store/primordial-dwarfism-market

Some of Primordial Dwarfism Companies are:

·         GeneScience Pharmaceuticals

·         Merck

·         Genentech, Inc.

·         Pfizer

·         Novo Nordisk

·         EMD Serono

·         And Many Others

Primordial Dwarfism Therapies are:

·         Jintrolong® low dose group

·         Recombinant human growth hormone (r-hGH)

·         Somatropin

·         And Many Others

To get more detailed insight about Primordial Dwarfism Therapies @Request for a Sample Report here: https://www.delveinsight.com/report-store/primordial-dwarfism-market

 

Sialidosis Market

Sialidosis is characterized by a deficiency of the digestive enzyme, alpha-neuraminidase. The lack of this enzyme results in an abnormal accumulation of complex carbohydrates known as mucopolysaccharides, and of fatty substances known as mucolipids. Both of these substances accumulate in bodily tissues. There are four types of Sialidosis: Each type of Sialidosis is characterized by the age of onset and by the type of physical and mental manifestations of this disorder.

Some of Sialidosis facts:

·         As per ISMRD, Sialidosis is among the rarest Lysosomal Storage Diseases, affecting perhaps less than 1:4,000,000 worldwide and is thought to be more common in people with Italian ancestry.

·         As per the International Advocate for Glycoprotein Storage Diseases (ISMRD), Type I is the mildest form of Sialidosis, with a range of onset from anywhere between 8-25 years of age.

·         According to NORD, Sialidosis affects males and females in equal number.

·         The prevalence is estimated to be less than 1/1,000,000.

View Report: https://www.delveinsight.com/report-store/sialidosis-market

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