Category: Metabolic / Miscellaneous Disorders

Ayurvedic Treatment For Ehlers Danlos Syndrome

ABSTRACT

Collagen is the most important protein present in the body and is hard, fibrous as well as insoluble. It is found in our skin, bones, muscles and tendons and helps in providing the body strength as well as elasticity. Fibroblast is the cell that is responsible for making 5 type of collagen including Type 1 is found in skin tendons, bones and organs, Type 2 is the home for cartilage, Type 3 is supporting mesh for the soft organs like blood vessels and liver, Type 4 is found in basal lamina on which the epithelial cells are found and Type 5 is found on the surface of cells like placenta and hair. The synthesis of Collagen is done by the gene called COL and there are many genes that encode different genes but what happens when these are defected it gives rise to a disorder known as Ehlers-Danlos Syndrome. Here through this article we are going to discuss this rare collagen disorder and its management through herbal medicine.

EHLERS DANLOS SYNDROME

WHAT IS EHLERS DANLOS SYNDROME

It is a group of inherited disorders that mainly affects the connective tissue and symptoms differ depending on the affected gene. Ehlers Danlos syndrome is mainly characterized by the joint hypermobility where the joints stretch more than normal, tissues are fragile and skin hyperextensibility where the person is able to stretch his or her skin more than normal. Currently it has been diagnosed that EDS has thirteen types and each type has its own clinical presentation. It is seen that one in every 5000 patients is affected with Ehlers Danlos Syndrome.

WHAT ARE THE TYPES AND CAUSES OF EDS

Here are the thirteen different type of EDS along with its cause

CLASSICAL EDS

The main symptoms of this type are

  • Atrophic Scarring
  • Skin Hyperextensibility
  • Generalized Joint Hypermobility.

Cause:-In more than 90 percent of cases with Classical EDS has heterozygous mutation where one of the genes encodes Type 5 collagen (COL5A1 and COL5A2). It is rarely seen that genes encoding the type 1 collagen are mutated and is an autosomal dominant type.

CLASSICAL-LIKE EDS

Symptoms seen are

  • The skin texture appears velvety along with presence of skin hyperextensibility and absence of atrophic scarring.
  • Easy bruising of skin and discoloration of the skin.
  • Recurrent dislocation of the joints

Cause:-This type is caused by the lack of Tenascin XB due to mutation of biallelic TNXB and this is the only gene related with Classical-like EDS. This is an autosomal recessive type.

CARDIAC-VALVULAR EDS

Here are the symptoms seen

  • Atrophic scarring
  • Skin becomes thin
  • Easy bruising
  • Skin hyperextensibility
  • Severe and progressive cardiac-valvular problem including mitral valve and aortic valve.
  • Restricted mobility of joints.

Cause:-It is mainly caused due to family history with autosomal recessive transmission, It is seen that there is a mutation of biallelic COL1A2 Collagen which results in lack of proa2-chain. This then leads to nonsense mediated mRNA decay and COL1A2 is the only one gene related to Cardiac Valvular EDS

VASCULAR EDS

There are the main symptoms seen in patient

  • Ruptured artery at very young age
  • Perforation of Sigmoid colon in the absence of known diverticular disease or other bowel disease.
  • Rupturing of Uterine walls during the 3rd trimester or severe perineum tear.
  • Formation of Carotid cavernous sinus fistula with the absence of trauma

Cause:-There is family history and is mostly seen in patients who are less than 40 year old.

The patient with Vascular EDS has heterozygous type of mutation on the COL3A1 gene and is autosomal dominant inherited.

HYPERMOBILE EDS

There are no specific symptoms seen in this type and the hypermobility also remains unidentified in most cases. It is the secondary manifestation of other types of EDS.

The underlying cause is yet to be discovered but it is autosomal dominant inherited.

ARTHROCHALASIA EDS

Main symptoms seen are

  • Hip dislocations
  • Multiple dislocations
  • Skin hyperextensibility

Cause:-It is caused due to mutation of heterozygous mutation of either COL1A1 OR COL1A2 gene. There is either half or entire loss of the xon 6 of the gene. This is an autosomal dominant and one of the rare types.

DERMATOSPARAXIS EDS

The main characteristic symptom is skin becomes very fragile and craniofacial symptoms.

Cause:-This is caused due to mutation of ADAMTS2 gene and is autosomal recessive.

KYPHOSCOLIOTIC EDS

Symptoms seen are

  • Abnormal curving of the spine
  • Dislocation of hip bone or knee bone
  • Congenital muscle hypotonia

Cause:-It is the mutation of the PLODI gene and is autosomal recessive dominant.

BRITTLE CORNEA SYNDROME:-

Symptoms presented are

  • The cornea becomes thin with or without being ruptured.
  • Progressive Keratoconus
  • Blue sclerae

Cause:- Brittle Cornea Syndrome is caused due to biallelic mutation of either PRDM5 or ZNF469 and is autosomal recessive dominant

SPONDYLODYSPLASIA EDS

Main clinical features seen are

  • Muscle hypotonia
  • Stature becomes short
  • Bowing of the limbs

Cause:- The cause for Spondylodysplasia EDS is yet to be known and is autosomal recessive dominant.

MUSCULOCONTRACTURAL EDS

Symptoms and signs seen are

  • Craniofacial features that are mostly seen at the time of birth or during early infancy.
  • Congenital multiple contractures which results in clubfoot and adduction-flexion contractures.
  • Skin Hyperextensibility
  • Easy bruising
  • Skin becomes fragile
  • Increased wrinkling

Cause:- Musculocontractural EDS is caused due to mutation of the CHST14 gene and is mainly autosomal recessive dominant.

MYOPATHIC EDS

Main signs and symptoms seen are

  • Muscle atrophy
  • Hypermobility of distal joints
  • Proximal joint contractures

Cause:- Myopathic EDS is caused due to heterozygous mutation of COL12A1 gene and can be inherited by both autosomal recessive and autosomal dominant patterns.

PERIODONTAL EDS

The signs and signature seen are

  • Pretibial Plaques
  • Lack of attached gingiva
  • Intractable periodontitis

Causes:- Periodontal EDS is caused due to heterozygous mutation of C1R or C15 gene and is autosomal dominant.

HOW EHLERS DANLOS SYNDROME CAN BE DIAGNOSED

There are many clinical diagnosis to rule out EDS and this includes

  • Genetic test
  • Echocardiogram
  • Skin Biopsy
  • Blood test

TREATMENT

According to modern science the treatment for Ehlers-Danlos syndrome is giving medications like Ibuprofen, naproxen sodium and acetaminophen which will only reduce the pain. As, there are no specific medications for EDS in modern science and the medication will only give temporary relief with other health complications.

In Ayurveda Ehlers-Danlos Syndrome is Correlated with Sehaj Dhatugad Vihar which is caused due to beej-beej bhav (Genetic or chromosomal defect). This results in disturbing the dhatu and this results in symptoms like Skin Hyperextensibility or hypermobility. Ayurveda provides herbal medicine which will help in the production of collagen naturally and making the skin as well as bones healthy. It will remove the root cause of the disease with any complications.

HERBAL MEDICINE PROVIDED BY PLANET AYURVEDA

Herbal remedies provided by Planet Ayurveda are 100 percent pure, natural and vegetarian which helps in balancing the Dosha as well as removing the root cause of the disease. Every Ayurvedic herb made under Planet Ayurveda is free from chemicals, preservatives and additives. All the herbal formulations are made under the supervision of an MD Ayurvedic Doctor and each of them are clinical.They all are free from side effects and safe to use as well. Here are the list of herbal medicine for Ehlers Danlos Syndrome:-

  1. Ashwagandha Capsules
  2. Shatavari Capsules
  3. Green Essentials
  4. Boswellia Curcumin
  5. Yograj Guggul
  6. Manjishtha Capsules


Ehlers–Danlos syndrome PackChronic Pelvic Pain And Prostatitis

Product Description

1. Ashwagandha Capsules

This herbal medicine is formed from a single herb known as Ashwagandha (Withania somnifera) which is one of the excellent remedies for providing the body with strength. Ashwagandha helps in providing the tissue with nourishment and particularly gives strength to the bones as well as muscles. It is the best herbal medicine for the nervous system which enhances the mental as well as physical activities.

Dosage:- One capsule twice daily after meals with water.

2. Shatavari Capsules

This herb is rich in antioxidant and anti-inflammatory properties made from Shatavari (Asparagus racemosus). It helps in boosting the immunity and making the body stronger. It is very beneficial in enhancing the production of collagen naturally and making it one of the effective medicine for EDS

Dosage:- One capsules after meals twice daily with water.

3. Green Essentials

This herbal medicine is formulated with Alfalfa (Medicago sativa), Amla (Embellica officinalis), Chlorella (Chlorella vulgaris), Spirulina (Spirulina platensis), Grape seed (Vitis vinifera), Green tea (Camellia sinensis) and many more. Green Essential will help in providing the body with all the nutrition that is required for collagen.

Dosage:- One capsule twice daily with plain water after meals.

4. Boswellia Curcumin

It is the combination of two excellent herbs like Shallaki (Boswellia serrata) and Curcumin (Curcuma longa). Boswellia Curcumin will not only help in promoting the circulation around the joint but will also strengthen the muscles as well.

Dosage:- One capsule twice daily with water after meals.

5. Yograj Guggul

It helps in pacifying the Vata Dosha as it contains herbs like Guggul (Commiphora mukul), Chitrak (Plumbago zeylanica), Ajwain (Carum copticum), Kulanjan (Alpinia galanga), Chavya (Piper Chaba), Rasna (Pluchea lanceolata), Haritaki (Terminalia chebula) and many more. All the formulated herbal remedies will help in reducing the pain and making the bones healthy.

Dosage:- One tablet with water twice a day after meals.

6. Manjishtha Capsules

It contains a single herb called Manjishtha (Rubia cordifolia) which helps in improving the circulation around the body. It helps in supporting the system and making the skin healthy as they become thin in EDS patients. They are also very effective in reducing anxiety, stress and depression.

Dosage:- One capsule twice daily with water after meals.

Some Healthy Tips

Include food and nutrients that will help in making the collagen healthy:-

  • Vitamin A:- Plant foods that have beta-carotene and other Vitamin-A  sources which are derived from animals.
  • Copper:- Include red meat, nuts, shellfish  in the diet and also consume drinking water.
  • Proline:- Eat soy, cabbage, meat and egg whites.
  • Vitamin C:- Include oranges, strawberries, broccoli and pepper
  • Anthocyanidins:- Include blueberries, cherries, raspberries and blackberries.

Conclusion

Ehlers Danlos syndrome is a rare genetic disorder as discussed above and can cause many health issues. In Allopathy there is no proper treatment for the EDS but Ayurveda provides their herbal medicine that helps in proper management of the disease. All the herbal remedies mentioned above will help in improving collagen production as well as making the bones strong. In case of any query kindly visit www.PlanetAyurveda.com

Natural Cure For Galloway Mowat syndrome

Galloway Mowat Syndrome

ABSTRACT

The trend of genetic diseases is increasing nowadays. One of such conditions is Galloway mowat syndrome. This is an extremely rare congenital disorder which is manifested by a variety of physical & neurological abnormalities along with an early onset of a series of renal disorders. In this article we’ll discuss the causes, symptoms, of this syndrome along with the Ayurvedic aspect & line of management of the disease with best Ayurvedic formulations.

Galloway Mowat Syndrome

INTRODUCTION

Galloway mowat syndrome is a neurodegenerative autosomal recessive condition present since birth and characterised by the variety of features including triad of microcephaly (when the newborn baby’s head is very smaller than the normal), hiatal hernia (a condition when the part of stomach bulges through the diaphragm in the chest cavity) along with nephrotic syndrome (multiple kidney related issues).

Galloway Mowat CAUSES

Galloway-Mowat syndrome appears to be genetically inheritable and is considered to be transmitted in an autosomal recessive fashion of inheritance, which means the defective gene for the syndrome is located on autosome and the both copies of genes (one from each parent) are necessary for the disorder’s manifestation. The individual/ parent who carries one of the mutated autosomes will not show any kind of sign & symptoms related to the disorder.

Multiple genes (10 genes) are believed to be the causative factors for the clinical manifestation of this syndrome, in which the significant cases have been shown to be caused by biallelic mutations in the WDR73 gene.

One gene, LAGE3, is associated with X-linked inheritance of Galloway Mowat syndrome.

SIGNS & SYMPTOMS

The cardinal features of this disorder as discussed above are

  • Microcephaly & neurological disturbances
  • Hiatal hernia
  • Nephrotic Syndrome

Other clinical features include:

  • Cognitive impairment
  • Delayed milestones.
  • Neuropathies (various nerve related disorders)
  • Digestion issues
  • Recurrent kidney & Urinary tract infections
  • Isolated proteinuria to full blown nephrotic syndrome in early stages.
  • Severe intellectual disability
  • Epilepsy, hypotonia, ataxia, spasticity and extrapyramidal dystonia.
  • Short stature, facial disfigurement
  • Hiatus hernia
  • Ocular abnormalities (progressive optic atrophy, nystagmus and strabismus).

Ayurvedic View

Acharya Charaka and mentioned the various congenital deformities that may be produced due to mutation in genes by following phrase:


Charka Sharir sthan-Shlok

(Reference— Charka Sharir sthan- 3/17)

Garbhoutpadak beej (sperm & ovum) and beej bhag (genes/chromosomes linked encoded within the sperm/ovum) are the basic ingredient for the formation of various tissues & organs, any kind of deformity (mutation) at the level of genes (beej bhag) will be responsible for the disorders related to that particular organs & organ systems.

TREATMENT

As the disease involves renal disorders, hiatal hernia and neurological symptoms.

The line of treatment for the disease include:

  • Use of herbs that provide strength to the kidney & urinary system.
  • Herbal formulations that strengthen the brain & nervous systems.
  • Digestion stimulating drugs
  • Immune boosting drugs
  • Dhatu poshak drugs (formulation that provide adequate nourishment to the child)

Herbal remedies Galloway mowat syndrome by Planet Ayurveda

Planet Ayurveda is the best herbal formulating company that makes products which are in strict adherence to the Ayurvedic principles and formulations as suggested by our acharyas in that ancient time hundreds of decade back. The herbs & minerals used for the formulation of various medicines are obtained from 100% natural sources. These are then duly processes, purified and formulated according to ancient time tested formulas under the guidance of our expert ayurvedic physicians.

Best herbal remedies as suggested by Planet Ayurveda for this Galloway mowat syndrome are:

  1. Punarnava Mandur
  2. Reno Plan Syrup
  3. Kumar Kalyan Ras
  4. Neuro Plan Syrup
  5. Digesto Plan Syrup

GallowayMowatsyndrome

PRODUCT DESCRIPTION

1. Punarnava Mandur

Punarnava Mandur is a classical preparation available in tablet form. The main ingredient here is Punarnava (Boerhavia diffusa) which is the best single drug for kidney, beneficial in improving kidney functions by providing strength to the kidney muscles. Along with it it also contains trikatu (combination of three pungent drugs i.e. Piper nigrum, Piper longum & Zingiber officinale) and mandur (detoxified iron ore) which collectively act as blood purifiers and help in the formation of new blood cells. Thus, reducing the load on the kidney this formulation helps in Galloway Mowat Syndrome.

Dosage: 1 tablet twice daily after feeding. (to be crushed well and then used with Reno Plan syrup)

2. Reno Plan Syrup

Reno Plan Syrup is the herbal syrup made by our team experts by combining the goodness of many herbs that promotes the kidney functions. The main ingredients of this syrup includes Punarnava, gokshura (Tribulus terrestris) and varun (Crataeva nurvala) which are the best herbal diuretics and are useful in preventing or treating various urinary tract infections. The distorted renal functions in this syndrome are well managed by the ingredient trin panchmool ghan vati which is an ayurvedic formulation made using 5 roots of grasses that are mutravirechak in action. The other ingredients such as Kalmegha (Andrographis paniculata), kaasni (Cichorium intybus) etc. aids in scavenging the free radicals by their antioxidant properties.

Dosage: 1 teaspoon twice daily after feeding.

3. Kumar Kalyan Ras

Kumar Kalyan Ras is the herbomineral compound which is described in the ancient Ayurvedic texts. This preparation is used in Galloway Mowat Syndrome due to the dhatu poshak (nourishing action on depleted bodily tissues) action of its ingredients. The ingredients of Kumar Kalyan Ras include swarna bhasma (purified ash of gold), abhrak bhasma (purified and processed ash of mica), shuddha parada (purified form of mercury), mukta bhasma (calx of pearl), loha bhasma (purified ash of iron) and makshika bhasma (purified extract of copper – iron pyrite) along with Kumari Rasa (Aloe vera’s juice extract). These calx of purified minerals are well efficient to reach upto the cellular level and nourish the various body tissues. Along with aloe vera which also facilitates in enhancing the immune system & maintaining hormonal balance.

Dosage: One tablet daily (to be chewed or crushed & used with syrup), after feeding.

4. Neuro Plan Syrup

Neuro Plan Syrup is the amazing poly herbal syrup made on the guidance of our expert team for the various neurological disorders. The herbs used in the syrup aids in calming the mental dosha i.e. raja & tama dosha. In this case i.e. Galloway mowat Syndrome is a neurodegenerative disorder in which there is a gradual decrease in neurological functions. Neuro Plan syrup’s ingredients such as Brahmi (Bacopa monnieri), Jyotishmati (Celastrus paniculatus), Mandukaparni (Centella asiatica) and Shankhpushpi (Convolvulus pluricaulis) etc. are the best medhya dravya (nervine tonics) and they strengthen the nervous system and also make the internal environment favourable for the proper functioning of brain & brain cells.

Dosage: 1 teaspoon two times a day after feeding.

5. Digesto Plan Syrup

Digesto Plan Syrup is the best herbal remedy for digestive issues & providing strength to abdominal musculature. In this case the major manifestation also includes hiatal hernia. So, this syrup will support the digestion of the baby & aiding in strengthening the muscles of the abdomen to prevent hernia from proceeding further. The ingredients include trikatu (Sonth, Maricha, Pippali) along with triphala i.e. combination of three fruits amalaki (Embilica officinalis), bibhitaki (Terminalia bellirica) and haritaki (Terminalia chebula) and other such herbs will make the digestion faster and also promote the cleansing action which will decrease the excessive  load or distension of the abdomen, which will prevent the hernia to pop out more further. Despite that it promotes the healing of hernia side by side by providing strength to those muscles.

Dosage– 1 tsp twice daily after feeding

CONCLUSION

It is very unlucky to have such a rare neurodegenerative disorder that affects multiple systems of the body. Despite giving steroids to the young child at very early stages of life which have tons of adverse effects in the later stages of life, use of such herbal based medicines is the best alternative for Galloway Mowat syndrome. For more information kindly visit www.PlanetAyurveda.com