Mental Health Conditions
SCN2A-related neurodevelopmental disorder
Serious
ICD-10: QA0 · NIH NLM
हिंदी: एससीएन2ए जीन विकार · தமிழ்: எஸ்சிஎன்2ஏ மரபணு கோளாறு · ಕನ್ನಡ: ಎಸ್ಸಿಎನ್2ಎ ಜೀನ್ ಅಸ್ವಸ್ಥತೆ · తెలుగు: ఎస్సిఎన్2ఏ జన్యు రుగ్మత · বাংলা: এসিএন2এ জিন ব্যাধি · मराठी: एससीएन2ए जनुक विकार · ગુજરાતી: એસસીએન2એ જનીન વિકાર
About this condition
SCN2A-related neurodevelopmental disorder is a genetic condition caused by changes in a gene that controls brain cell communication. Children may experience seizures starting in infancy, delayed milestones in walking and talking, and varying degrees of intellectual disability. Each affected individual has unique symptoms requiring personalized medical management and supportive therapies.
Common symptoms
developmental delays
seizures
intellectual disability
speech delay
autism-like behaviors
movement problems
feeding difficulties
When to see a doctor: immediately upon recognizing developmental delays or seizures
This condition in Indian languages
| Hindi (हिंदी) | एससीएन2ए जीन विकार · बच्चों में मिर्गी और विकास में देरी · दौरे और बौद्धिक अक्षमता · जन्मजात मस्तिष्क विकार |
| Tamil (தமிழ்) | எஸ்சிஎன்2ஏ மரபணு கோளாறு · குழந்தைகளில் வலிப்பு மற்றும் வளர்ச்சி தாமதம் · மூளை வளர்ச்சி குறைபாடு · நரம்பு வளர்ச்சி பிரச்சனை |
| Kannada (ಕನ್ನಡ) | ಎಸ್ಸಿಎನ್2ಎ ಜೀನ್ ಅಸ್ವಸ್ಥತೆ · ಮಕ್ಕಳಲ್ಲಿ ಸೆಳೆತ ಮತ್ತು ಬೆಳವಣಿಗೆ ವಿಳಂಬ · ಮೆದುಳಿನ ಬೆಳವಣಿಗೆ ದೋಷ · ನರ ಬೆಳವಣಿಗೆ ಸಮಸ್ಯೆ |
| Telugu (తెలుగు) | ఎస్సిఎన్2ఏ జన్యు రుగ్మత · పిల్లల్లో మూర్ఛలు మరియు అభివృద్ధి ఆలస్యం · మెదడు అభివృద్ధి లోపం · నాడీ అభివృద్ధి సమస్య |
| Bengali (বাংলা) | এসিএন2এ জিন ব্যাধি · শিশুদের খিঁচুনি এবং বিকাশ বিলম্ব · মস্তিষ্ক বিকাশের ত্রুটি · স্নায়ু বিকাশ সমস্যা |
| Marathi (मराठी) | एससीएन2ए जनुक विकार · मुलांमध्ये अपस्मार आणि विकास विलंब · मेंदू विकास दोष · मज्जासंस्था विकास समस्या |
| Gujarati (ગુજરાતી) | એસસીએન2એ જનીન વિકાર · બાળકોમાં આંચકી અને વિકાસ વિલંબ · મગજ વિકાસ ખામી · ચેતા વિકાસ સમસ્યા |
Frequently asked questions
What are the symptoms of SCN2A-related neurodevelopmental disorder?
developmental delays, seizures, intellectual disability, speech delay, autism-like behaviors, movement problems.
When should I see a doctor?
immediately upon recognizing developmental delays or seizures
Is SCN2A-related neurodevelopmental disorder common in India?
This condition is seen across India.
How serious is SCN2A-related neurodevelopmental disorder?
Severity is classified as Serious. immediately upon recognizing developmental delays or seizures.
Related conditions
Important: This information is for general awareness only and is
not a substitute for professional medical advice. Always consult a qualified doctor.
In an emergency, call 112.
Data sourced from NIH NLM
and MOHFW India.
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