Tricho-dento-osseous syndrome, often shortened to TDO, is a rare inherited disorder that affects the hair, the teeth and the bones. It follows an autosomal dominant pattern, is present from birth, and is caused by a mutation in the DLX3 gene, which helps control how hair follicles differentiate and how bone forms. Everyone with the syndrome has enamel hypoplasia and taurodontism, so the teeth are discolored, thin, pitted or fragile and may be malformed inside and out. Hair is rough and sheds heavily, often curly in infancy and straighter later. Some people have an underbite, a prominent lower jaw and longer bones. Cases have clustered in families and in nearby areas of Virginia, Tennessee and North Carolina. Care is team based, drawing on dentists, physical therapists and oral and maxillofacial surgeons, with genetic counseling and emotional support recommended. This record is a reference summary of what is documented, not medical advice.
Facts
Classification
ICD-10 ChapterXVII: Congenital Malformations, Deformations and Chromosomal Abnormalities 2 Communicable or Non-communicable Transmission Route Causative Agent
Causative Agent (category) Prevalence Band Sources
1. Tricho-dento-osseous syndrome (Wikipedia)
Lead
Tricho-dento-osseous syndrome (TDO) is a rare, systemic, autosomal dominant genetic disorder that causes defects in hair, teeth, and bones respectively.
Lead, first paragraph
causes defects in hair, teeth, and bones
Lead, first paragraph [causative-agent-category]
The cause of this disease is a mutation in the DLX3
Lead, first paragraph [disease-category]
autosomal dominant genetic disorder
View the Source2. Orphadata (Orphanet): Orphadata cross-references for ORPHA:3352 Tricho-dento-osseous syndrome
Orphadata (Orphanet)ICD-10 cross-referenceQuote, ICD-10 cross-reference
"Reference": "Q82.4", "Source": "ICD-10"
View the Source 3. Orphadata (Orphanet): Orphadata: Epidemiology of rare diseases (en_product9_prev)
Orphadata (Orphanet)ORPHA:3352Quote, ORPHA:3352
Point prevalence Class only <1 / 1 000 000
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