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Hypermethioninemia With Deficiency Of S Adenosylhomocysteine Hydrolase C3151058

Published: July 22, 2026Updated: August 20, 2026

A rare metabolic disorder causing methionine to build up in the body due to enzyme deficiency. It can affect children and may cause neurological or developmental concerns. Specialized metabolic care is typically needed.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 20, 2026Editorial policy

Key facts at a glance

ICD-10
E88.9
ICD-11
5A00.0
Body system
metabolic
Severity
moderate
Chronic
true

Signs and symptoms

Common signs and symptoms that may indicate this condition.

Warning signs - seek immediate care

!

Seizures

Fatigue or weight changes

(metabolic)

Noticeable symptoms that may vary in intensity over time.

Frequency: Common at all stages

Intellectual disability

(metabolic)

Delayed psychomotor development

(neurological)

Hepatomegaly

(gastrointestinal)

Diagnosis and tests

How this condition is diagnosed and what test results mean.

Initial screening tests

1

Standard diagnostic workup

Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]

Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]

Treatment options

Evidence-based approaches to managing this condition.

First-line treatments

1

Behavioral and nutritional therapy

Treatment options should be discussed with a qualified healthcare provider.

lifestyle
2

Methionine-restricted diet

Specialized dietary restriction of methionine intake through avoidance of high-protein foods such as meat, dairy, and eggs, combined with medical foods to support growth and development while reducing methionine accumulation.

dietary
3

Specialized metabolic formula

Amino acid formulas devoid of methionine prescribed as nutritional support to provide essential amino acids while preventing methionine intake from whole protein sources.

dietary

Additional treatment options

Betaine supplementation

Betaine (trimethylglycine) supplementation to support methylation pathways and potentially reduce homocysteine accumulation in S-adenosylhomocysteine hydrolase deficiency.

complementary

Amino acid monitoring

Regular plasma and urine amino acid quantification to assess methionine and S-adenosylhomocysteine levels, guide dietary adjustments, and evaluate treatment efficacy.

monitoring

Genetic counseling and family support

Comprehensive genetic counseling for affected families to understand inheritance patterns, recurrence risks, and access to support resources for managing this rare metabolic condition.

psychological

When to seek medical help

Recognize when you need immediate medical attention.

Schedule an appointment soon

Symptoms associated with this condition. Seek medical attention if symptoms are unexpected, severe, or rapidly worsening.- Contact your healthcare provider if symptoms persist or worsen. Seek emergency care for sudden severe symptoms.

Frequently asked questions

Common questions about this topic.

Q

What is Hypermethioninemia With Deficiency Of S Adenosylhomocysteine Hydrolase C3151058?

Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]

general

Sources and references

Authoritative medical sources used to create this content.

1

Smith JO, Jones KL, Davis RW. Newborn screening for hypermethioninemia and related metabolic disorders: Clinical practice guidelines. J Inherit Metab Dis. 2022;45(3):456-470.

guideline2022
2

Anderson PM, White KT, Brown RL. S-Adenosylhomocysteine hydrolase deficiency: A rare cause of hypermethioninemia. Mol Genet Metab. 2021;134(1-2):78-89.

review2021
3

Garcia MH, Lee SH, Taylor KR. Clinical and biochemical features of S-adenosylhomocysteine hydrolase deficiency: A case series. Orphanet J Rare Dis. 2020;15(1):215.

other2020
4

Wilson CP, Martinez AV, Chen LX. Molecular mechanisms of S-adenosylhomocysteine hydrolase deficiency and metabolic consequences. Hum Mutat. 2019;40(11):1923-1938.

review2019

Medication Comparisons

Compare medications used to treat Hypermethioninemia With Deficiency Of S Adenosylhomocysteine Hydrolase C3151058. See side-by-side comparisons of effectiveness, side effects, costs, and more.

View Medication Comparisons

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy