Genetic Evaluation

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At our clinic, we specialize in the identification and diagnosis of Lysosomal Disorders (LD) and a wide range of genetic conditions. Our approach is designed to address the complexities of medical issues that remain undiagnosed or fall outside conventional disease classifications.

Comprehensive Genetic Diagnoses and Care for Lysosomal Disorders and Genetic Diseases

Our Diagnostic Journey:

Step 1: Personalized Consultation - Your journey begins with an in-depth consultation with one of our experienced physicians. Here, we'll take a comprehensive medical history and develop a three-generation family tree to better understand potential genetic influences.

Step 2: Thorough Physical Examination - Following the consultation, you'll undergo a detailed physical examination. This includes an assessment of dysmorphology to identify any physical anomalies, and a complete neurological evaluation to check for any neurological concerns.

Step 3: Genetic Testing and Analysis - We employ a tiered approach to genetic testing, starting with traditional methods and progressing to more targeted molecular or cytogenetic tests as needed. This process is complemented by the latest in genetic and genomic technology, ensuring that we explore all avenues for diagnosis.

Our goal is to provide a comprehensive evaluation that sheds light on complex medical mysteries, paving the way for tailored treatment plans and support. With our dedicated team and advanced diagnostic tools, we're committed to delivering the highest standard of care for our patients and their families

Connect with us

LDRTC

3702 Pender Drive, Suite 170,
Fairfax VA 22030