Townes–Brocks syndrome: Difference between revisions

Townes–Brocks syndrome
Synonyms	TBS
Pronounce
Specialty	Medical genetics
Symptoms	Imperforate anus, dysplastic ears, thumb anomalies, hearing loss, renal abnormalities
Complications	N/A
Onset	Congenital
Duration	Lifelong
Types	N/A
Causes	Genetic mutation in the SALL1 gene
Risks	Family history of the condition
Diagnosis	Clinical evaluation, genetic testing
Differential diagnosis	VACTERL association, CHARGE syndrome, Fanconi anemia
Prevention	N/A
Treatment	Symptomatic management, surgery for anatomical anomalies
Medication	N/A
Prognosis	Variable, depending on severity of symptoms
Frequency	Rare
Deaths	N/A

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Latest revision as of 19:31, 8 April 2025

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Townes–Brocks syndrome (TBS) is a rare genetic disorder characterized by a triad of congenital anomalies: anorectal malformations, ear abnormalities, and thumb malformations. It is an autosomal dominant condition, meaning that a single copy of the altered gene in each cell is sufficient to cause the disorder.

Etiology[edit]

Townes–Brocks syndrome is caused by mutations in the SALL1 gene, which provides instructions for making a protein that is involved in the development of many parts of the body. The SALL1 protein is a transcription factor that regulates the activity of other genes, particularly during embryonic development.

Clinical Features[edit]

The clinical presentation of Townes–Brocks syndrome can vary widely among affected individuals, even within the same family. The most common features include:

Anorectal malformations: These can range from mild anal stenosis to more severe forms such as imperforate anus.
Ear abnormalities: These may include preauricular tags, hearing loss, and structural ear defects.
Thumb malformations: These can include triphalangeal thumbs, duplicated thumbs, or hypoplastic thumbs.

Other possible features include renal anomalies, cardiac defects, and genitourinary abnormalities.

Diagnosis[edit]

Diagnosis of Townes–Brocks syndrome is based on clinical findings and can be confirmed by genetic testing to identify mutations in the SALL1 gene. Prenatal diagnosis is possible if the mutation in the family is known.

Management[edit]

Management of Townes–Brocks syndrome is symptomatic and supportive. It may involve surgical correction of anorectal malformations, hearing aids for hearing loss, and orthopedic interventions for limb anomalies. Regular monitoring of renal function and cardiac health is also recommended.

@@ Line 1: / Line 1: @@
-== Townes–Brocks Syndrome ==
+{{SI}}
+{{Infobox medical condition
-[[File:Autosomal_dominant_-_en.svg|thumb|right|Diagram of autosomal dominant inheritance pattern.]]
+| name            = Townes–Brocks syndrome
+| image           = [[File:Autosomal_dominant_-_en.svg|200px]]
+| caption         = Townes–Brocks syndrome is inherited in an [[autosomal dominant]] pattern.
+| synonyms        = TBS
+| pronounce       =
+| specialty       = [[Medical genetics]]
+| symptoms        = [[Imperforate anus]], [[dysplastic ears]], [[thumb anomalies]], [[hearing loss]], [[renal abnormalities]]
+| onset           = Congenital
+| duration        = Lifelong
+| causes          = [[Genetic mutation]] in the [[SALL1]] gene
+| risks           = Family history of the condition
+| diagnosis       = [[Clinical evaluation]], [[genetic testing]]
+| differential    = [[VACTERL association]], [[CHARGE syndrome]], [[Fanconi anemia]]
+| treatment       = Symptomatic management, [[surgery]] for anatomical anomalies
+| prognosis       = Variable, depending on severity of symptoms
+| frequency       = Rare
+}}
 '''Townes–Brocks syndrome''' (TBS) is a rare [[genetic disorder]] characterized by a triad of [[congenital anomalies]]: [[anorectal malformations]], [[ear abnormalities]], and [[thumb malformations]]. It is an [[autosomal dominant]] condition, meaning that a single copy of the altered gene in each cell is sufficient to cause the disorder.
 === Etiology ===
 Townes–Brocks syndrome is caused by mutations in the [[SALL1]] gene, which provides instructions for making a protein that is involved in the development of many parts of the body. The SALL1 protein is a transcription factor that regulates the activity of other genes, particularly during embryonic development.
 === Clinical Features ===
 The clinical presentation of Townes–Brocks syndrome can vary widely among affected individuals, even within the same family. The most common features include:
 * '''Anorectal malformations''': These can range from mild anal stenosis to more severe forms such as imperforate anus.
 * '''Ear abnormalities''': These may include preauricular tags, hearing loss, and structural ear defects.
 * '''Thumb malformations''': These can include triphalangeal thumbs, duplicated thumbs, or hypoplastic thumbs.
 Other possible features include [[renal anomalies]], [[cardiac defects]], and [[genitourinary abnormalities]].
 === Diagnosis ===
 Diagnosis of Townes–Brocks syndrome is based on clinical findings and can be confirmed by genetic testing to identify mutations in the SALL1 gene. Prenatal diagnosis is possible if the mutation in the family is known.
 === Management ===
 Management of Townes–Brocks syndrome is symptomatic and supportive. It may involve surgical correction of anorectal malformations, hearing aids for hearing loss, and orthopedic interventions for limb anomalies. Regular monitoring of renal function and cardiac health is also recommended.
+== See also ==
-== Related Pages ==
 * [[Genetic disorder]]
 * [[Autosomal dominant]]
 * [[Congenital anomaly]]
 * [[SALL1]]
 {{Genetic disorders}}
 [[Category:Genetic disorders]]
 [[Category:Congenital disorders]]