What is Noma?
Noma, also known as cancrum oris or gangrenous stomatitis, is a severe, rapidly progressive gangrenous infection of the mouth and face. It is not a genetic disorder but rather an infectious disease that predominantly affects malnourished children, typically between the ages of 2 and 6 years, living in conditions of extreme poverty and poor sanitation, primarily in sub-Saharan Africa. The disease is classified under Orphanet code 2700 and ICD-10 code A69.0. Noma begins as a small ulcer or lesion on the gingiva (gums) or oral mucosa, often following a debilitating illness such as measles, malaria, or other infections that compromise the immune system. The infection rapidly spreads, causing destruction of the soft and hard tissues of the face, including the lips, cheeks, nose, and jaw bones. The gangrenous process can perforate through the skin, leading to devastating facial disfigurement. Without treatment, noma has a mortality rate estimated at approximately 90%. Key predisposing factors include severe malnutrition, poor oral hygiene, immunosuppression, and recent infectious illness. Treatment of noma requires early detection and prompt intervention. In the acute phase, management includes broad-spectrum antibiotics (such as amoxicillin or metronidazole), nutritional rehabilitation, wound care, and treatment of underlying conditions. Survivors of the acute phase are often left with severe facial deformities, including trismus (inability to open the mouth), which require complex reconstructive surgery. Prevention strategies focus on improving nutrition, oral hygiene, vaccination programs, and access to healthcare in at-risk populations. In 2023, the World Health Organization added noma to its list of neglected tropical diseases, increasing global awareness and efforts toward prevention and treatment.
Also known as:
- Age of Onset
- Childhood
- Begins in childhood, roughly ages 1 to 12
FDA & Trial Timeline
1 eventData is compiled from FDA regulatory filings and ClinicalTrials.gov, then processed through automated extraction; event classifications and dates may occasionally be misclassified. Verify against the linked FDA filing or trial record before clinical decisions. Updated periodically.
Treatments
Source: openFDA + DailyMed · NDA / BLA labels with structured indications · refreshed weekly
No FDA-approved treatments are currently listed for Noma.
1 clinical trialare actively recruiting — trials can provide access to cutting-edge therapies.
View clinical trials →Source: ClinicalTrials.gov · synced daily · phases, status, and PI names normalized at ingest
Source: NPI Registry + PubMed · trial PI roles cross-referenced with ClinicalTrials.gov · ranked by match score (publications + PI activity + community signal)
Treatment Centers
8 centersSource: NORD Rare Disease Centers + NIH Undiagnosed Diseases Network (UDN) · centers verified active within last 12 months
Children's Hospital Colorado Rare Disease Program ↗
Children's Hospital Colorado
📍 Aurora, CO
👤 Boston Children's Hospital Rare Disease Program
🔬 UDNHarvard/MGH UDN Clinical Site ↗
Massachusetts General Hospital
📍 Boston, MA
🏥 NORDBoston Children's Hospital Rare Disease Program ↗
Boston Children's Hospital
📍 Boston, MA
👤 Boston Children's Hospital Rare Disease Program
🏥 NORDUCLA Rare Disease Day Program ↗
UCLA Health
📍 Los Angeles, CA
🏨 Children'sAnn & Robert H. Lurie Children's Hospital Genetics ↗
Lurie Children's Hospital
📍 Chicago, IL
👤 Boston Children's Hospital Rare Disease Program
🏥 NORDCincinnati Children's Hospital Medical Center ↗
Cincinnati Children's
📍 Cincinnati, OH
👤 Boston Children's Hospital Rare Disease Program
🏨 Children'sNationwide Children's Hospital Rare Disease Center ↗
Nationwide Children's Hospital
📍 Columbus, OH
👤 Boston Children's Hospital Rare Disease Program
🔬 UDNNIH Clinical Center Undiagnosed Diseases Program ↗
National Institutes of Health
📍 Bethesda, MD
Travel Grants
No travel grants are currently matched to Noma.
Community
No community posts yet. Be the first to share your experience with Noma.
Start the conversation →Latest news about Noma
Source: PubMed + NIH RePORTER + openFDA + clinical-journal RSS · last 30 days · disease-tagged at ingest by AI extraction with human QC
Disease timeline:
New recruiting trial: Real-time NOMA Evaluation
A new clinical trial is recruiting patients for Noma
Caregiver Resources
NORD Caregiver Resources
Support, advocacy, and financial assistance for caregivers of rare disease patients.
Mental Health Support
Rare disease caregiving can be isolating. Connect with counseling and peer support.
Family & Caregiver Grants
Financial assistance programs specifically for caregivers of rare disease patients.
Social Security Disability
Learn how rare disease patients may qualify for SSDI/SSI benefits.
Common questions about Noma
What is Noma?
Noma, also known as cancrum oris or gangrenous stomatitis, is a severe, rapidly progressive gangrenous infection of the mouth and face. It is not a genetic disorder but rather an infectious disease that predominantly affects malnourished children, typically between the ages of 2 and 6 years, living in conditions of extreme poverty and poor sanitation, primarily in sub-Saharan Africa. The disease is classified under Orphanet code 2700 and ICD-10 code A69.0. Noma begins as a small ulcer or lesion on the gingiva (gums) or oral mucosa, often following a debilitating illness such as measles, malar
At what age does Noma typically begin?
Typical onset of Noma is childhood. Age of onset can vary across affected individuals.
Are there clinical trials for Noma?
Yes — 1 recruiting clinical trial is currently listed for Noma on UniteRare. See the clinical trials section on this page for phase, sponsor, and site details sourced from ClinicalTrials.gov.
Which specialists treat Noma?
1 specialists and care centers treating Noma are listed on UniteRare, sourced from ClinicalTrials.gov principal investigators, published research, and the NPPES NPI registry.
Frequently asked questions about Noma
Auto-generated from canonical disease facts (Orphanet, OMIM, ClinicalTrials.gov, openFDA, NPPES). Not a substitute for clinical guidance.
What is Noma?
Noma is a rare disease catalogued in international rare-disease ontologies (Orphanet ORPHA:2700). Inheritance pattern depends on the specific subtype. Age of onset is generally childhood. For verified primary sources, see the UniteRare Noma page.
Are there FDA-approved treatments for Noma?
Approved treatments for Noma are tracked from openFDA and DailyMed primary sources. Many rare diseases have no specific FDA-approved therapy; for those, supportive care and management of complications form the basis of clinical care. Orphan-drug-designation status is noted where applicable.
Are there clinical trials recruiting for Noma?
UniteRare currently lists 1 clinical trial relevant to Noma sourced from ClinicalTrials.gov. Each trial entry includes recruitment status, eligibility criteria summary, principal-investigator information, and study locations. Patients should discuss eligibility with their healthcare provider before enrolling.
How do I find a specialist for Noma?
UniteRare lists 1 verified clinician with documented expertise in Noma, sourced from ClinicalTrials.gov principal-investigator records, PubMed publication histories, and the NPPES NPI registry. Filter by state or browse our state-specific specialist pages for nearby options.
See full Noma page for complete clinical details, sources, and verified-specialist listings.
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