Disease⁚ Say-Carpenter syndrome Overview of the Disease Carpenter syndrome is a rare genetic disorder characterized […]
Understanding Chromosome 1 Deletion: Genetic Basis, Symptoms, and Management
Understanding the Genetic Basis Understanding the genetic basis of chromosome 1 deletion is crucial․ This […]
Understanding Canavan Leukodystrophy: Causes, Symptoms, Diagnosis, Treatment, Research, Prognosis, and Support
Causes of Canavan Leukodystrophy Canavan leukodystrophy is primarily caused by a mutation in the ASPA […]
Understanding Candidiasis Familial Chronic
In this section, we explore the causes, symptoms, treatment, diagnosis, prevention, and more of this […]
Understanding ARVD Symptoms, Genetic Inheritance, and Treatment Options
Palpitations and Irregular Heartbeat Fainting Spells or Syncope Chest Pain and Discomfort Palpitations and Irregular […]
Understanding Polysyndactyly Microcephaly Ptosis Syndrome
Introduction This article discusses Polysyndactyly Microcephaly Ptosis‚ a syndrome characterized by unique features affecting multiple […]
Overview of Polysyndactyly, Trigonocephaly, and Agenesis of Corpus Callosum
Today’s information discusses a case of an 11-month-old boy with a pattern of anomalies including […]
Home Remedies for the Common Cold
Home Remedies for the Common Cold Exploring the difference between cold and flu․ How to […]
Introduction to Polysyndactyly Cardiac Malformation
Syndrome with characteristics of polysyndactyly‚ hexadactyly‚ and complex cardiac malformation has been described in patients․ […]
Overview of Polysyndactyly type Haas
Polysyndactyly type Haas is characterized by complete syndactyly of all fingers with polydactyly‚ resulting in […]