Journal of Rare Disorders: Diagnosis & Therapy Insight Medical Publishing is entirely committed to provide the most accurate and innovative source of online learning, transforming and advancing science, health and technology. For science to function effectively, and for society to reap full benefits from scientific endeavors, it is crucial that science data be made open. Thus, we work on the open-access, author- pay model and provide peer-reviewed content with the support of lead researchers and thinkers in the cadre. Insight Medical Publishing holds comprehensive journals in its archive and shares a proactive approach to give an efficient and effective output to enhance their credibility. Formed in 2005, is appreciated today for delivering the most relevant and outstanding science to the scientists, researchers and general masses from then. Journal of Rare Disorders: Diagnosis & Therapy Volume 8, Issue 5 https:/ The ReceptorBinding Component of Anthrax Toxin Elicits ToxinNeutralizing Antibodies Which Provide Protection against Anthrax Disease Dereje Birhanu https:/ Retroperitoneal Sarcomas A Heterogeneous Group of Malignancies of Mesenchymal Origin Developing From Retroperitoneal Tissues and Vessels Sarah Watson https:/ A Rare Neurodevelopmental Disorder with an Extensive Phenotypic Variability Resulting In a Challenging Clinical Diagnosis Anne Chiaramello https:/ Mandibular Hypoplasia Deafness Progeroid Highlights and Lipodystrophy Condition Is an Uncommon Autosomal Prevailing Problem Alexis Tarrada https:/ Aeromonas Hydrophila Is a Significant Oceanic Zoonotic Microorganism That Causes Septicemia Shao Jun Tang Journal of Rare Disorders: Diagnosis & Therapy Volume 10, Issue 1 https:/ Splenic Hepatic and Gastric Sarcoidosis Case Study Nawal Lagdali, Camelia Berhili, Maryeme Kadiri, Fatima Zahra Habib, Imane Benelbarhdadi, Mohamed Borahma and Fatima Zahra Ajana https:/ Adolescent Health and Wellbeing in Sickle Cell Disease Marcos Bezerra https:/ Rare Muscular Disorder Research and Treatment Hanns Lochmller https:/ Cushings Syndrome Causes Symptoms Diagnosis and Treatment Gul Ilhan https:/ Genomic Sequencings Impact on Rare Disease Diagnosis Sandra Cooper https:/ The Role of i FEM1B i in a Rare Syndromic Neurodevelopmental Disorder Brook Meyer https:/ Advancements in Precision Medicine From Rare Diseases to Complex Syndromes Klein Haneveld https:/ Cryopreserved Allogenic Bone Marrow Relocate inside Paediatric Population Kimberlee Hanna https:/ Examination of Gene Mutation Attributes and its Connection with Prognosis in Patients Haiping Zhang https:/ Multielement Examination of Single Red Platelets Amin Haq Journal of Rare Disorders: Diagnosis & Therapy Volume 9, Issue 6 https:/ Musculoskeletal Disorders in the Practice of Physical Therapy Ali Tahir https:/ Metabolic Disorders and Complexity of Human Metabolism Chandan Mazumdar https:/ Factors Effecting the Importance of Enigma in Rare Genetic Mutations Rui Sousa https:/ Advancement of Intriguing Endocrine Issues Rasoul Goli https:/ Causes and Types of Chromosomal Abnormalities that Leads to Health Conditions Naijun Tang https:/ Nucleic Acid Drugs and Quality Therapies Silvia Girotti https:/ Rare Congenital Disorders and the Human Experience Vronique Debien https:/ Medical Procedure Works on Endurance of Uncommon Urinary Malignant Growths Daniel Orbach https:/ Frequency of Stroke in a Brazilian Population with Sickle Cell Anaemia Mrio Luiz https:/ An Efficient Planning Survey between Taking Care of Wild Meat and Zoonotic Sicknesses Sameeh Abutarbush Journal of Rare Disorders: Diagnosis & Therapy Volume 9, Issue 5 https:/ Genomic Ways to Deal with Rare Disorder Analysis Maxi Thomas https:/ Unusual Uterine Draining in the Young Adults Margaret Ragni https:/ Women with Abnormal Bleeding Disorders during Menstrual Bleeding Frank Leebeek https:/ Expanding Horizons in Therapeutic Design for Nervous System Diseases Navid Faraji https:/ AIDS Dementia Complex with Positive 1433 Protein in Cerebrospinal Fluid A Case Report and Literature Reviewa Yunsen He1, Xiaohong Qin2, Min Feng4, Qinjiang Huang3, Mengjun Zhang2, Lili Guo1, Mingbin Bao1, Ye Tao1, Hongyuan Dai3, and Bo Wu1 https:/ A Rare Disease with Premature Aging Case Report Cansu Erel, Cemil Tascioglu Journal of Rare Disorders: Diagnosis & Therapy Volume 9, Issue 4 https:/ The Genetic Complexity of Rare Blood Disorders Inmaculada Aban https:/ Rare Skin Disorders and Diseases Daniel Bracey https:/ Beyond Hemophilia Understanding Rare Blood Disorders Syed Jaja https:/ Pantothenate KinaseAssociated Neurodegeneration The Dystonia with Eyes Disorder Luke Mart https:/ Fields Syndrome The Mystery Muscle Disorder Abiona Oluwadamilola https:/ Proteus Syndrome The Elephant Mans Curse John Wood https:/ Stiff Person Syndrome The Human Statue Disorder V Degos https:/ Unlocking the Mysteries of Sickle Cell Anemia A Comprehensive Exploration Suzanne Sap https:/ The Impact of Muscular Dystrophy on Patients and Families Markus Rantala Journal of Rare Disorders: Diagnosis & Therapy Volume 9, Issue 3 https:/ Enigma Syndrome Unraveling the Mysteries of a Rare Disorder Krick Sanan https:/ Predominance of Hemorrhagic Ovarian Sores in Patients with Uncommon Acquired Draining Issues Jessica David https:/ High Prevalence of Heavy Menstrual Bleeding In Women with Rare Bleeding Disorders Krister Fjermestad https:/ Information Mentalities and Practices of Canine toward Zoonotic Illnesses David Pigott https:/ The Worldwide Weight of Ignored Zoonotic Sicknesses Hanul Thukral https:/ Ct Imaging for an Interesting Instance of Subcutaneous PanniculitisLike Immune System Microorganism Lymphomatosis Marcelo Correia https:/ Precious Stone Blackfan Iron Deficiency in GrownUps In Pursuit of a Common Approach for a Rare Disease Steven Holloway https:/ An Uncommon Femoral Heterotopic Bone Development in Female Skeleton Joana Garcia https:/ Langerhans Cell Histiocytosis of the Front Facing Bone with Unforeseen Appearances Pranay Tanwar https:/ Bone Marrow Metastasis of Testicular Microorganism Cell Growth Vikash Reebye Journal of Rare Disorders: Diagnosis & Therapy Volume 9, Issue 1 https:/ Late Disclosures in the Pathology and SubAtomic Investigation of the Most Relentless RPS Subtypes John Watson https:/ Lipodystrophy Condition is an Exceptional Autosomal Winning Issue Accomplished by Changes in POLD1 Quality Arun Goyal https:/ Chromosomal Irregularities can Work with Tumorigenesis and Change the Cell Wellbeing Dinesh Kane https:/ Mental Stressors are Average Wagered Factors for Supportive Neurological Issue Ali Khalid https:/ Electrocardiography for Risk Portrayal in Patients with Brugada Condition Sushmitha Rao https:/ General Perspectives and Chance Impression of Zoonotic Sicknesses Ciamarra Anna https:/ Focusing on Zoonotic Illnesses is one of the Significant Errands Laura Hadi https:/ Uncommon NUS1 Variations Altogether Enhanced in Parkinsons disease Mary Bellgard https:/ An Uncommon Hereditary Disorder with Multisystem Contribution Mirco Mannino https:/ Irresistible and Noninfectious Eye Conditions Connected with Basic Foundational Illness Howard Dongmei Journal of Rare Disorders: Diagnosis & Therapy Volume 8, Issue 12 https:/ Uneven Extension of the Epiphyseal Ligament of the Long Bones German Coussens https:/ Vagrant Medication Advancement in the Area of Dermatology Chang Helena https:/ Neurometabolic Diseases Are Complex Group of Rare Neurogenetic Disorders Sisinthy Xiang https:/ Beneficial Effects in Patients with Ocular Allergies and Some Studies Gabriel Erin https:/ Toward An Understanding of Mcardle Disease A CrossSectional International Questionnaire Study Stacey L Reason1, Renee Cadzow2, Briana J Jegier3, Amy Nwora4, Alejandro Lucia5, Andrew Wakelin6, RM Quinlivan7 and Nicol C Voermans8 Journal of Rare Disorders: Diagnosis & Therapy Volume 8, Issue 11 https:/ To Investigate the Opportunity of Treatment Influence Heterogeneity in Craftsmanship Patients Aras Meredith https:/ Harm in the Alveolar Recruitment for Acute Respiratory Distress Syndrome Trial Christoph S https:/ Alternative Option In Drug Development and Is Often Presented As Being A Viable Daniel Giustra https:/ Challenge of Current Biomedicine Is To Identify Curative Therapies for Every Disease in a Personalized Way Darby Schmidt https:/ To Avoid the Recurrence of Myeloma Multiplex And Due To the Frequent and Serious Angioedema Attacks Henriette Farkas Journal of Rare Disorders: Diagnosis & Therapy Volume 8, Issue 10 https:/ The neutralizing epitopes of the rabies virus and the neutralization mechanism of monoclonal antibodies Baoqing Sun https:/ Pretreatment and posttreatment of rottlerin effectively reduce the viral replication of ZIKV Wei Wang https:/ Q fever is a zoonotic disease caused by Coxiella burnetii which causes abortions in domestic ruminants Jesper Garg https:/ campylobacteriosis ranks as one of the most frequently reported foodborne illnesses Michael Lake https:/ Chromosomal abnormalities in aged eggs indicating that ovulation reduction slows the aging of oocytes Daniel Kane Journal of Rare Disorders: Diagnosis & Therapy Volume 8, Issue 8 https:/ Aspiratory cryptococcosis is the commonest area of nonfocal sensory system cryptococcosis Liming Zhang https:/ A Few Investigations Investigate the Viral System of Sickness Movements and Its General Pathogenesis Shibnath Dev https:/ Quality Level Corpus Commented on with Uncommon Illnesses and Their Clinical Signs Erin Luonan https:/ Chronic Inflammatory Disorders of the Digestive Tract And They Involve Systemic Inflammatory Diseases Tito Xiaosheng https:/ What is Barth Tired A Qualitative Approach to Understanding Fatigue in Barth Syndrome from the Perspective of Family Members Stacey Reynolds, Emma Daw, Isabelle Babson and Virginia Way Tong Chu Journal of Rare Disorders: Diagnosis & Therapy Volume 8, Issue 7 https:/ Obtrusive Histoplasmosis Is the Most WellKnown AIDSCharacterizing Occasion in Endemic Areas Nathalie Ghorra https:/ Pneumonic Blastomycosis Is a Respiratory Sickness That Is Brought About By the Parasite Blastomyces Spp Christopher Chew https:/ Uncommon Illnesses Allude To Sicknesses with Exceptionally Low Predominance Lin Chau Chang https:/ Qualitative Investigation of Fatigue and Its Daily Impacts as Perceived by Individuals with Barth Syndrome Isabelle Babson, Emma Daw and Stacey Reynolds https:/ Traumatic Ventral Cord Herniation Presenting with Sexual Dysfunction A Case Report and Review of Literature Omar AlAwar2,4, Georgio Haddad2,3, Tarek Bou Dargham3, Mohamad Bahij Moumneh3, Elias Horanieh3, Christine Atallah3, Mira Bou Ayache5, Marwan M Haddad6 and ChurlSu Kwon1 Journal of Rare Disorders: Diagnosis & Therapy Volume 8, Issue 6 https:/ Chromosomal Irregularities Comprising Of Mathematical and Underlying Chromosome Irregularities Are a Typical Quality of Disease Daniel Kane https:/ NonTransmittable Infections That Essentially either Inordinate or Diminished Discharge of Chemicals Mohammad Salimullah https:/ Electro cardiology assumes a Significant Part in Recognizing the Objective Site on the Right Half of the Septum Mohamad Alkhouli https:/ Eyes See What Mind Knows Fibrodysplasia Ossificans Progressiva a Mimicker of Spondyloarthritis Roshila Shamim1, Asadullah Khan2, Saira Elaine Anwer Khan3, Muhammad Zeeshan Aslam4 and ArfaTalia5 https:/ A Rare Case of an Intrapancreatic Gastric Duplication Cyst as the Cause of Recurrent Pancreatitis Literature Review of Gastric Duplication Cysts in Adult Population Konstantinos S Flamourakis1, Nikolaos Memos1, Dimitrios P Bouklas2, Despoina Myoteri2, Manousos M Konstadoulakis1 and Dina G Tiniakos2 Journal of Rare Disorders: Diagnosis & Therapy Volume 8, Issue 9 https:/ Granulomas Are a Pathological Sign of Histoplasmosis but They Can Also Be Found In Sarcoidosis Ahmed Ahmed https:/ Histoplasmosis is Mistakenly Diagnosed as Miliary Tuberculosis in NonEndemic Regions Suha Abu Khalaf https:/ Molecular Factors That Are Responsible For the Pathogenesis of Endometriosis Liangcai Hou https:/ Role that metabolism of carbohydrates and lipids plays in the etiology and pathogenesis of MS David Kadosh https:/ UCD Case Report Glycerol Phenylbutyrate in the Management of Female Patients with Ornithine Transcarbamylase Deficiency Sharan Goobie, Gabriella Horvath and Shailly JainGhai Journal of Rare Disorders: Diagnosis & Therapy Volume 8, Issue 4 https:/ Target Innervation and Typically Cocooning Cell Demise Darren Samuel https:/ Intrigued Individuals Own Muscles John Herld https:/ Advancement and Authoritative Intercessions are Important to Decrease the Gamble David kaka https:/ Kinematic Technique of Instant Centre Analysis of the Knee Yu lee https:/ Essential System for Speeding up the Decrease in Youngster Mortality Tim Cook Journal of Rare Disorders: Diagnosis & Therapy Volume 8, Issue 3 https:/ Bronchial Discharges from the More Unassuming Periphery Li Weng https:/ Chipping Away at Persevering Responsibility in Continuous Recuperation Tony Lee https:/ Implantation for Portrayal of Powerful Cycles Naina Willams https:/ Functional Outcomes than Their More Energetic Accomplices Qi Chen Li https:/ Essential Determination of Myocardial Dead Tissue Shang chi Journal of Rare Disorders: Diagnosis & Therapy Volume 8, Issue 2 https:/ A Rare Disorder Masking an Underlying Anorectic Carcinoma Jennifer Gladys Mulle https:/ Brain Development Through the Lens of Rare Genetic Disorders Martyna Zaleska https:/ A Rare Disorder of Thermoregulation Astrid Schielke Mard hand https:/ Children with Autism Spectrum Disorder and Rare Diseases Tara Chand Saini https:/ Child Behaviors Positively Predict Symptoms of Posttraumatic Stress Alexandra Schnabel Journal of Rare Disorders: Diagnosis & Therapy Volume 8, Issue 1 https:/ Abnormal Melatonin Secretion May Play a Role in Sleep Disturbance pspan stylefontsize100ptspan stylelineheight115span stylefontfamilyquotCalibriquot,quotsansserifquotEmma C Woodfordspanspanspanp https:/ Advances in Genomics Biology Gene Editing and Gene Delivery pspan stylefontsize100ptspan stylelineheight115span stylefontfamilyquotCalibriquot,quotsansserifquotHuLin Jiang spanspanspanp https:/ Rare Monogenic Disorders are a Group of SingleGeneMutated Diseases pspan stylefontsize100ptspan stylelineheight115span stylefontfamilyquotCalibriquot,quotsansserifquotYuKyoung Ohspanspanspanp https:/ Brain is the most Important Part of the Central Nervous System pspan stylefontsize100ptspan stylelineheight115span stylefontfamilyquotCalibriquot,quotsansserifquotFeng Zhen Wangspanspanspanp https:/ Configuration of each Stereo Genic Center is Determined Singly pspan stylefontsize100ptspan stylelineheight115span stylefontfamilyquotCalibriquot,quotsansserifquotKrister W Fjermestadspanspanspanp Journal of Rare Disorders: Diagnosis & Therapy Volume 7, Issue 10 https:/ Insights on Hairy Cell Leukemia pElisha Stewartp https:/ A Report on Inherited Metabolic Disorders pElisha Stewartp https:/ Editorial Note on Chronic Granulomatous Disease pElisha Stewartp https:/ Editorial Note on Retroperitoneal Fibrosis pElisha Stewartp https:/ Next Generation Sequencing Unusual Cases of Spastic Paraplegic Presenting with Ataxia pPriyanka Vishwakarma,nbspSarita Agarwal,nbspDeepika Delsa Dean andnbspKausik Mandalp Journal of Rare Disorders: Diagnosis & Therapy Volume 7, Issue 9 https:/ Pulmonary Manifestations and the Effectiveness of Enzyme replacement in Fabry Disease with the pR227X Mutation pPaumlivi PietilaumlEffatisup1sup,nbspnbspJohan Soumlderstroumlmsup2nbspsup, Jukka T Saarinensup3sup,nbspEliisa Loumlyttyniemisup4sup,nbspIlkka Kantolasup5supp https:/ Insights of Congenital Heart Disease pElisha Stewartp https:/ Insights on Multiple Myeloma Myelodyspastic Syndrome pElisha Stewartp https:/ Editorial on the Cancer Biomarkers pElisha Stewartp https:/ Editorial on Pernicious Anaemia pElisha Stewartp Journal of Rare Disorders: Diagnosis & Therapy Volume 7, Issue 8 https:/ Large Granular Leukemia a Lympho Proliferative Disorder pElisha Stewartp https:/ Amyotrophic Lateral Sclerosis pElisha Stewartp https:/ Histiocytosis of Langerhans Cells pElisha Stewartp https:/ Editorial on Biopsy of Muscle pElisha Stewartp https:/ Editorial on Acute Spinal Cord Injury pElisha Stewartp Journal of Rare Disorders: Diagnosis & Therapy Volume 7, Issue 7 https:/ Editorial on Cushings Disease pSophia Robertsp https:/ Editorial on Diabetes Insipidus pSophia Robertsp https:/ Duchenne Muscular Dystrophy pSophia Robertsp https:/ Adrenal Insufficiency Addison Disease pSophia Robertsp https:/ Thoughts on the Application of High Flow Nasal Cannula Oxygen Therapy in Patients with Severe Pneumonia A Case Report and Review of Literature pDezhu Tang, Xiaohui Zhou, KeXiong Lin, and Yun Wanp Journal of Rare Disorders: Diagnosis & Therapy Volume 7, Issue 6 https:/ Alice in Wonderland Syndrome pSophia Robertsp https:/ Urea Cycle Disorders pSophia Robertsp https:/ Progressive Familial Intrahepatic Cholestasis pSophia Robertsp https:/ Editorial on Moebius Syndrome pSophia Robertsp https:/ Editorial on Pfeiffer Syndrome pSophia Robertsp Journal of Rare Disorders: Diagnosis & Therapy Volume 9, Issue 2 https:/ Unveiling the Complexity of Rare Congenital Disorders Dominique Heinke https:/ Rare Vascular Disorders Understanding the Uncommon Weizhong Yang https:/ Rare Cancer A Challenge in Diagnosis Treatment and Research MartinsFilho https:/ Orphan Drugs Addressing Unmet Medical Needs William Taylor https:/ Zoonotic Diseases The Intersection of Humans and Animal Health Anindita Banerjee https:/ A Right Hypochondrial Discharging Sinus not to be MissedSpontaneous Cholecystocutaneous Fistula A R M Isthiyak and Anura SK Banagala https:/ Acquired Deafness Have Colossally Perceived the Basic Atomic Pathways Meghan Harry https:/ Youngsters with Phenomenal Diseases in School Presents Inconveniences Castilla Berta https:/ The Improvement of Transient Solutions for Remarkable Neurological Disorders Flora Leesa https:/ Hydatid Disorder is a Regular Sickness Requiring Cautious Intercession Alberto Escarpa Journal of Rare Disorders: Diagnosis & Therapy Volume 7, Issue 5 https:/ Editorial on LeschNyhan Disease pSophia Robertsp https:/ Psychology and Branches of Psychology pSophia Robertsp https:/ Editorial on Psychopathy pSophia Robertsp https:/ Insights of Burkitt Lymphoma pSophia Robertsp https:/ Attention Deficit Hyperactivity Disorder pSophia Robertsp