Science Communication
As an Associate Medical Writer at Klarity Health, I author clear, evidence‑based articles on genetics, rare diseases and healthy living. Below is a selection of my recent publications. Click any title to read the full article on Klarity Health.
Growth Patterns in PURA Syndrome
A look at why children with PURA syndrome experience failure to thrive and short stature and how clinicians can support them.
Fragile X Syndrome in Adulthood
Explores employment challenges and independent living for adults with Fragile X syndrome and the supports available.
Pathophysiology of Pyoderma Gangrenosum
Discusses the role of neutrophils and inflammation in the development of this rare, painful skin disorder.
Etiology of Transient Neonatal Pustular Melanosis
Explains the possible causes and contributing factors behind this benign newborn skin condition.
The Influence of Genetics on Cardiomegaly
A guide to identifying at‑risk populations for an enlarged heart and how genetic factors contribute to the condition.
Distinguishing Treacher Collins Syndrome
Outlines how to differentiate Treacher Collins syndrome from other craniofacial disorders for accurate diagnosis.
Differential Diagnosis of Gitelman Syndrome
Provides an overview of this rare kidney disorder and how to distinguish it from similar electrolyte conditions.
Genetic Basis of Barakat Syndrome
Examines the genetic mutations behind this complex triad disorder and their clinical implications.
Proton Therapy for Spinal Tumours
An introduction to proton therapy and how it offers precise treatment with fewer side effects for spinal tumours.
The Role of CBD in Migraine Pain
Discusses how cannabidiol may help manage migraine pain intensity when traditional therapies fall short.
Psychodynamic Therapy for Eating Disorders
Explores how psychodynamic therapy can support recovery from disorders like anorexia, bulimia and binge‑eating.
For the complete archive of my work, visit my author page on Klarity Health.
Full Writing Archive
All of my published articles and writing samples — click to expand.
Clinical Presentation of Tumoral Calcinosis
Tumoral calcinosis (TC) is a rare inherited medical condition in which calcium and phosphate builds up in the soft tissues around joints.
Complications of Tay-Sachs Disease
Tay-Sachs disease is a rare and fatal genetic disorder that primarily affects the nervous system.
Cri Du Chat Syndrome and Sleep Disturbances
Exploring the relationship between Cri du Chat syndrome and the sleep challenges faced by affected individuals.
Differential Diagnosis of Gitelman Syndrome
Gitelman Syndrome (GS) is a rare genetic disorder that affects the kidneys' ability to process certain electrolytes.
Etiology and Mechanisms of TTTS in Monochorionic Pregnancies
Twin-to-Twin Transfusion Syndrome (TTTS) is a severe and potentially life-threatening condition in monochorionic twin pregnancies.
Etiology of Transient Neonatal Pustular Melanosis
Possible causes and contributing factors behind this benign newborn skin condition.
Fragile X Syndrome in Adulthood
Fragile X Syndrome (FXS) is the most common inherited cause of intellectual disability and autism spectrum disorder.
Genetic and Familial Forms of Left Bundle Branch Block
Left bundle branch block (LBBB) is a common cardiac conduction abnormality characterised by delayed electrical conduction.
Genetic Basis of Barakat Syndrome
Barakat syndrome is a rare genetic disorder that affects multiple organ systems.
Genetic Counseling for Frontonasal Dysplasia
The importance of genetic counselling for families affected by frontonasal dysplasia.
Genetic Factors in Femoral Facial Syndrome
Femoral-Facial Syndrome (FFS) is a rare and complex congenital disorder presenting unique challenges.
Genital Warts and HPV Vaccine
Understanding the risks associated with HPV and the role of vaccination in prevention.
Genotype-Phenotype Correlations in Lissencephaly Subtypes
Lissencephaly is a developmental disorder characterised by a lack of standard folds in the brain.
Growth Patterns in PURA Syndrome
PURA syndrome is a rare genetic condition that affects brain development and often causes developmental delays.
Insulin Therapy for Children
Insulin therapy is an essential part of managing diabetes for many children.
Lavender's Potential for Alleviating Headaches
Exploring the potential of lavender as a natural remedy for headache relief.
Musculoskeletal Anomalies in Freeman-Sheldon Syndrome
Freeman-Sheldon Syndrome presents a complex array of physical challenges and musculoskeletal anomalies.
Music Therapy for Pain Management
Music therapy is an evidence-based practice that utilises music to achieve therapeutic goals.
Pathophysiology of Pyoderma Gangrenosum
The role of neutrophils and inflammation in pyoderma gangrenosum.
Prognosis and Recovery Timeline for Thigh Contusion Injuries
Thigh contusions are common injuries, particularly among athletes and active individuals.
Prolactinoma and Weight Gain
Prolactinoma can have far-reaching effects on various aspects of health including weight management.
Proton Therapy for Spinal Tumours
Precision in treating spinal tumours with proton therapy.
Psychosocial Impact of Batten Disease
Batten disease is a group of inherited disorders characterised by neuronal ceroid lipofuscinosis.
PUPPP Rash and Twin Pregnancy
PUPPP is an uncommon skin condition that affects some women during the late stages of pregnancy.
Psychodynamic Therapy for Eating Disorders
Eating disorders are complex psychiatric illnesses manifesting in extreme emotions and behaviours around food.
The Influence of Genetics on Cardiomegaly
Understanding genetic predisposition to cardiomegaly and identifying at-risk populations.
The Role of CBD in Managing Migraine Pain Intensity
How cannabidiol may help manage migraine pain when conventional treatments fall short.
What Is Klippel-Trenaunay Syndrome
Klippel-Trenaunay Syndrome (KTS) is an extremely rare congenital condition characterised by vascular malformations.
What Is Ornithine Translocase Deficiency
Also known as HHH syndrome, this is a rare but serious genetic disorder.
What Is Proteus Syndrome
Proteus syndrome is a rare congenital disorder characterised by mosaic overgrowth of tissues.
What Is Thoracic Aortic Aneurysm
A thoracic aortic aneurysm is characterised by abnormal dilation of the aorta in the chest area.
What Is Tietze Syndrome
Tietze syndrome is a medical condition with unique characteristics warranting comprehensive exploration.
What Is Tricuspid Valve Repair and Replacement
The tricuspid valve maintains proper blood flow through the heart.
What Is Valvuloplasty
A valvuloplasty is a procedure that repairs and widens narrowed heart valves.
What Makes Li-Fraumeni Syndrome Different
How Li-Fraumeni syndrome differs from other inherited cancer syndromes like BRCA1 or Lynch syndrome.
Where to Find Support in Your Weight Loss Journey
Exploring the support systems available for individuals on a weight loss journey.