Acute pharyngitis refers to inflammation of the pharynx (the throat space behind the nasal cavity and mouth). Acute pharyngitis is most commonly cause...
MAC Lung Disease – Symptoms, Treatment and Homeopathy Management
MAC Lung Disease is caused by a group of bacteria called MAC (Mycobacterium Avium Complex). These bacteria reside naturally in dust, soil, and water, ...
Dupuytren’s Contracture: Understanding Symptoms, Causes & Homeopathic Solutions
Dupuytren’s contracture is a chronic condition that involves the connective tissue (fascia) of the palm of the hand. The fascia becomes thickene...
Brachydactyly – Understanding Its Causes, Types & Homeopathy Treatment
Brachydactyly Meaning Brachydactyly (BD) is a birth defect in which the fingers or toes are shorter than usual because of underdeveloped or abnormal...
Hallermann Streiff Syndrome: Symptoms, Causes & Homeopathy Treatment
Hallermann-Streiff Syndrome (HSS) is a rare genetic disorder that affects physical and craniofacial development. It is characterized by distinctive fa...
Parry Romberg Syndrome- Causes, Symptoms & Homeopathy Treatment
Parry-Romberg Syndrome (PRS) is a rare, progressive condition characterized by the slow deterioration (atrophy) of the skin and soft tissues, usually ...
Pulmonary Alveolar Proteinosis- Causes, Symptoms & Homeopathy Treatment
Pulmonary Alveolar Proteinosis (PAP) is a rare lung disease characterized by the accumulation of surfactant (a fatty protein substance) in the alveoli...
Understanding Acyanotic Heart Disease: Causes, Symptoms, and Treatment
The heart is one of the most important organs of our body, pumping oxygen-rich blood to every organ. Some people are born with structural heart defect...
Ribose-5- Phosphate Isomerase Deficiency – Causes, Symptoms & Homeopathy Treatment.
Ribose-5-phosphate isomerase (RPI) deficiency is caused by mutations in the RPIA gene, which provides instructions for making the enzyme ribose-5-phos...
Schinzel-Giedion Syndrome -Causes, Symptoms & Homeopathy Treatment
Schinzel-Giedion Syndrome (SGS) is a rare genetic disorder caused by mutations in the SETBP1 gene. It is characterized by severe developmental delays,...