Hypotrichosis–lymphedema–telangiectasia syndrome
| Hypotrichosis–lymphedema–telangiectasia syndrome | |
|---|---|
| Synonyms | |
| Pronounce | N/A |
| Specialty | N/A |
| Symptoms | Sparse hair, lymphedema, telangiectasia |
| Complications | |
| Onset | |
| Duration | |
| Types | |
| Causes | Genetic mutation |
| Risks | |
| Diagnosis | Clinical examination, genetic testing |
| Differential diagnosis | |
| Prevention | |
| Treatment | Symptomatic treatment |
| Medication | |
| Prognosis | |
| Frequency | |
| Deaths | |
Alternate Names[edit]
Hypotrichosis lymphedema telangiectasia syndrome; HLTS; Hypotrichosis-lymphedema-telangiectasia-membranoproliferative glomerulonephritis syndrome; Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome
Definition[edit]
Hypotrichosis-lymphedema-telangiectasia syndrome (HLTS) is a rare condition that, as the name suggests, is associated with sparse hair (hypotrichosis), lymphedema, and telangiectasia, particularly on the palms of the hands.
Cause[edit]
HLTS is thought to be caused by changes (mutations) in the SOX18 gene.
Inheritance[edit]
It can follow both an autosomal dominant or an autosomal recessive pattern of inheritance, depending on the affected family.
Symptoms[edit]
For most diseases, symptoms will vary from person to person. People with the same disease may not have all the symptoms listed. 80%-99% of people have these symptoms
- Abnormality of the lymphatic system
- Absent eyebrow (Failure of development of eyebrows)
- Absent eyelashes(Failure of development of eyelashes)
- Alopecia(Hair loss)
- Palmar telangiectasia
- Plantar telangiectasia
- Predominantly lower limb lymphedema
- Sparse body hair
- Sparse scalp hair(Reduced/lack of hair on scalp)
30%-79% of people have these symptoms
- Cutis marmorata
- Hydrocele testis
- Palpebral edema(Fullness of eyelids)
5%-29% of people have these symptoms
- Ascites(Accumulation of fluid in the abdomen)
- Dermal atrophy(Skin degeneration)
- Hydrops fetalis
- Pleural effusion
- Fluid around lungs
Treatment[edit]
There is currently no cure for the condition. Treatment is based on the signs and symptoms present in each person.
| Genetic disorders relating to deficiencies of transcription factor or coregulators | ||||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|

This article is a dermatology stub. You can help WikiMD by expanding it!
NIH genetic and rare disease info[edit]
Hypotrichosis–lymphedema–telangiectasia syndrome is a rare disease.
| Rare and genetic diseases | ||||||
|---|---|---|---|---|---|---|
|
Rare diseases - Hypotrichosis–lymphedema–telangiectasia syndrome
|
Ad. Transform your health with W8MD Weight Loss, Sleep & MedSpa

Tired of being overweight?
Special offer:
Budget GLP-1 weight loss medications
- Semaglutide starting from $29.99/week and up with insurance for visit of $59.99 and up per week self pay.
- Tirzepatide starting from $45.00/week and up (dose dependent) or $69.99/week and up self pay
✔ Same-week appointments, evenings & weekends
Learn more:
- GLP-1 weight loss clinic NYC
- W8MD's NYC medical weight loss
- W8MD Philadelphia GLP-1 shots
- Philadelphia GLP-1 injections
- Affordable GLP-1 shots NYC
|
WikiMD Medical Encyclopedia |
Medical Disclaimer: WikiMD is for informational purposes only and is not a substitute for professional medical advice. Content may be inaccurate or outdated and should not be used for diagnosis or treatment. Always consult your healthcare provider for medical decisions. Verify information with trusted sources such as CDC.gov and NIH.gov. By using this site, you agree that WikiMD is not liable for any outcomes related to its content. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates, categories Wikipedia, licensed under CC BY SA or similar.
Translate this page: - East Asian
中文,
日本,
한국어,
South Asian
हिन्दी,
தமிழ்,
తెలుగు,
Urdu,
ಕನ್ನಡ,
Southeast Asian
Indonesian,
Vietnamese,
Thai,
မြန်မာဘာသာ,
বাংলা
European
español,
Deutsch,
français,
Greek,
português do Brasil,
polski,
română,
русский,
Nederlands,
norsk,
svenska,
suomi,
Italian
Middle Eastern & African
عربى,
Turkish,
Persian,
Hebrew,
Afrikaans,
isiZulu,
Kiswahili,
Other
Bulgarian,
Hungarian,
Czech,
Swedish,
മലയാളം,
मराठी,
ਪੰਜਾਬੀ,
ગુજરાતી,
Portuguese,
Ukrainian


