Quick access to resources and clinical support for inherited metabolic disorders.
Get Started as a Patient
Access medical foods, formulas, and specialized nutrition support for patients and families impacted by rare metabolic disorders. We provide bridge supplies, home monitoring tools, and case management until you’re able to establish sustainable access.
Disorders we support:
- Aminoacidopathies (PKU, Tyrosinemia, MSUD, HCU, Hypermethioninemia)
- Fatty acid oxidation disorders (CUD, LCHADD, MCADD, TFP, VLCAD, CPT1/2)
- Glycogen storage disorders (GSD I, III, IV)
- Lysosomal storage disorders
- Mitochondrial disorders
- Organic acid disorders (BKT, Cbl A/B/C, GA1/2, HMG, IVA, 3MCC, MCD, MMA, PA)
- Urea cycle disorders (OTC, Citrullinemia, ASA, Arginase, CPS, HHH)
- Other inherited metabolic disorders (Galactosemia, Biotinidase deficiency, and more)
Who’s eligible: Georgia residents or Emory Genetics Clinic patients with diagnosed inherited metabolic disorders.
Clinical Care from Newborn to Adulthood
Community Support & Programming
Our multidisciplinary team provides nutrition support from newborn screening through lifelong care. Services include rapid newborn screening follow-up, personalized meal planning, growth monitoring, and life transition support.
How we connect:
- In-person visits at Emory University
- Telemedicine consultations for families across Georgia
- Virtual support groups and peer connections
- Mobile-friendly resources and remote monitoring support
- Educational workshops on nutrition management skills
Access WIC benefits for medical foods across 20+ Georgia counties, join our 30-year Metabolic Camp program for young women with PKU and MSUD, and participate in real research studies that advance IMD treatment.
Check WIC Eligibility | Visit MetCamp Website | View Research Opportunities
MNT4P's Recipe Corner
Low-protein recipes for amino acid disorders and low-fat recipes for fatty oxidation disorders. Discover meal ideas, cooking tutorials, and tips for adapting recipes to your dietary needs.