Lamb-Shaffer syndrome: Difference between revisions
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[[File:Autosomal_dominant_-_en.svg| | {{SI}} | ||
{{Infobox medical condition | |||
| name = Lamb-Shaffer syndrome | |||
| image = [[File:Autosomal_dominant_-_en.svg|200px]] | |||
| caption = Lamb-Shaffer syndrome is inherited in an [[autosomal dominant]] manner. | |||
| synonyms = [[SHANK3-related disorder]] | |||
| field = [[Medical genetics]] | |||
| symptoms = [[Developmental delay]], [[intellectual disability]], [[speech delay]], [[autism spectrum disorder]] | |||
| onset = [[Infancy]] | |||
| duration = [[Lifelong]] | |||
| causes = [[Genetic mutation]] in the [[SHANK3]] gene | |||
| risks = [[Family history]] of the condition | |||
| diagnosis = [[Genetic testing]], [[clinical evaluation]] | |||
| differential = [[Autism spectrum disorder]], [[Phelan-McDermid syndrome]] | |||
| treatment = [[Supportive care]], [[speech therapy]], [[occupational therapy]] | |||
| prognosis = [[Variable]], depends on severity of symptoms | |||
| frequency = Rare | |||
| deaths = Not directly life-threatening | |||
}} | |||
'''Lamb-Shaffer syndrome''' (LSS) is a rare genetic disorder characterized by developmental delay, intellectual disability, and distinctive facial features. It is caused by mutations in the [[SOX5]] gene, which plays a crucial role in the development of the brain and other organs. | |||
== Presentation == | == Presentation == | ||
Individuals with Lamb-Shaffer syndrome typically present with a range of symptoms, including: | Individuals with Lamb-Shaffer syndrome typically present with a range of symptoms, including: | ||
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* Distinctive facial features such as a broad forehead, deep-set eyes, and a wide mouth | * Distinctive facial features such as a broad forehead, deep-set eyes, and a wide mouth | ||
* Behavioral issues, including autism spectrum disorder | * Behavioral issues, including autism spectrum disorder | ||
== Genetics == | == Genetics == | ||
Lamb-Shaffer syndrome is caused by mutations in the [[SOX5]] gene located on chromosome 12. The [[SOX5]] gene is part of the SOX (SRY-related HMG-box) family of transcription factors, which are involved in the regulation of embryonic development and cell fate determination. Mutations in this gene disrupt normal development, leading to the symptoms observed in LSS. | Lamb-Shaffer syndrome is caused by mutations in the [[SOX5]] gene located on chromosome 12. The [[SOX5]] gene is part of the SOX (SRY-related HMG-box) family of transcription factors, which are involved in the regulation of embryonic development and cell fate determination. Mutations in this gene disrupt normal development, leading to the symptoms observed in LSS. | ||
== Diagnosis == | == Diagnosis == | ||
Diagnosis of Lamb-Shaffer syndrome is typically made through genetic testing, which can identify mutations in the [[SOX5]] gene. Clinical evaluation of the patient's developmental history, physical examination, and assessment of facial features also contribute to the diagnosis. | Diagnosis of Lamb-Shaffer syndrome is typically made through genetic testing, which can identify mutations in the [[SOX5]] gene. Clinical evaluation of the patient's developmental history, physical examination, and assessment of facial features also contribute to the diagnosis. | ||
== Management == | == Management == | ||
There is currently no cure for Lamb-Shaffer syndrome. Management focuses on addressing the individual symptoms and may include: | There is currently no cure for Lamb-Shaffer syndrome. Management focuses on addressing the individual symptoms and may include: | ||
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* Behavioral therapy for autism spectrum disorder | * Behavioral therapy for autism spectrum disorder | ||
* Regular follow-up with a multidisciplinary team of healthcare providers | * Regular follow-up with a multidisciplinary team of healthcare providers | ||
== Epidemiology == | == Epidemiology == | ||
Lamb-Shaffer syndrome is a rare condition, with only a limited number of cases reported in the medical literature. The exact prevalence is unknown. | Lamb-Shaffer syndrome is a rare condition, with only a limited number of cases reported in the medical literature. The exact prevalence is unknown. | ||
== See also == | == See also == | ||
* [[SOX5]] | * [[SOX5]] | ||
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* [[Intellectual disability]] | * [[Intellectual disability]] | ||
* [[Autism spectrum disorder]] | * [[Autism spectrum disorder]] | ||
== References == | == References == | ||
{{Reflist}} | {{Reflist}} | ||
== External links == | == External links == | ||
{{No external links}} | {{No external links}} | ||
[[Category:Genetic disorders]] | [[Category:Genetic disorders]] | ||
[[Category:Rare diseases]] | [[Category:Rare diseases]] | ||
[[Category:Developmental disorders]] | [[Category:Developmental disorders]] | ||
[[Category:Neurological disorders]] | [[Category:Neurological disorders]] | ||
{{medicine-stub}} | {{medicine-stub}} | ||
Latest revision as of 00:41, 8 April 2025

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Obesity, Sleep & Internal medicine
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| Lamb-Shaffer syndrome | |
|---|---|
| Synonyms | SHANK3-related disorder |
| Pronounce | N/A |
| Specialty | N/A |
| Symptoms | Developmental delay, intellectual disability, speech delay, autism spectrum disorder |
| Complications | N/A |
| Onset | Infancy |
| Duration | Lifelong |
| Types | N/A |
| Causes | Genetic mutation in the SHANK3 gene |
| Risks | Family history of the condition |
| Diagnosis | Genetic testing, clinical evaluation |
| Differential diagnosis | Autism spectrum disorder, Phelan-McDermid syndrome |
| Prevention | N/A |
| Treatment | Supportive care, speech therapy, occupational therapy |
| Medication | N/A |
| Prognosis | Variable, depends on severity of symptoms |
| Frequency | Rare |
| Deaths | Not directly life-threatening |
Lamb-Shaffer syndrome (LSS) is a rare genetic disorder characterized by developmental delay, intellectual disability, and distinctive facial features. It is caused by mutations in the SOX5 gene, which plays a crucial role in the development of the brain and other organs.
Presentation[edit]
Individuals with Lamb-Shaffer syndrome typically present with a range of symptoms, including:
- Developmental delay
- Intellectual disability
- Speech and language impairment
- Distinctive facial features such as a broad forehead, deep-set eyes, and a wide mouth
- Behavioral issues, including autism spectrum disorder
Genetics[edit]
Lamb-Shaffer syndrome is caused by mutations in the SOX5 gene located on chromosome 12. The SOX5 gene is part of the SOX (SRY-related HMG-box) family of transcription factors, which are involved in the regulation of embryonic development and cell fate determination. Mutations in this gene disrupt normal development, leading to the symptoms observed in LSS.
Diagnosis[edit]
Diagnosis of Lamb-Shaffer syndrome is typically made through genetic testing, which can identify mutations in the SOX5 gene. Clinical evaluation of the patient's developmental history, physical examination, and assessment of facial features also contribute to the diagnosis.
Management[edit]
There is currently no cure for Lamb-Shaffer syndrome. Management focuses on addressing the individual symptoms and may include:
- Early intervention programs for developmental delays
- Special education services
- Speech and language therapy
- Behavioral therapy for autism spectrum disorder
- Regular follow-up with a multidisciplinary team of healthcare providers
Epidemiology[edit]
Lamb-Shaffer syndrome is a rare condition, with only a limited number of cases reported in the medical literature. The exact prevalence is unknown.
See also[edit]
References[edit]
<references group="" responsive="1"></references>
External links[edit]
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