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What type of Waardenburg syndrome is cleft lip most common?
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What is an integumentary disorder such as Waardenburg syndrome?
it is a large genatalia wart that only some men grow on the tip of there penis it is a large genatalia wart that only some men grow on the tip of there penis Waardenburg syndrome is a genetic disorder effecting hair, eye, facial pigment. It can effect facial features too such a shape of lips, nose bridge, eyebrows. It is most definitely not a genitalia , genital wart.
How is Velo cardio facial syndrome detected?
Velocardiofacial syndrome (VCFS) is a disorder that has been associated with over thirty different features. The name velocardiofacial syndrome comes from the Latin words "velum" meaning palate, "cardia" meaning heart and "facies" having to do with the face. Velocardiofacial syndrome may also be known as Shprintzen syndrome, DiGeorge syndrome, Craniofacial syndrome or Conotruncal Anomaly Unusual Face Syndrome. Get more information about Velocardiofacial syndrome at http://velocardiofacial-syndrome.blogspot.com Thanks
What is the prevalence of cleft lip in the population?
Cleft lip is the second most common embryonic deformity. Cleft lip occurs in approximately one in 750-1,000 live births.
How do you get cleft palate?
The condition is congenital; that is, babies who have cleft lip, cleft palate, or both are born with the condition. For more information, see: http://familydoctor.org/online/famdocen/home/children/parents/special/birth/034.htmlit is a birth defect
What is the most common nerve entrapment syndrome?
Carpal tunnel syndrome.
Waardenburg syndrome?
DefinitionWaardenburg syndrome is a group of inherited conditions characterized by deafness and partial albinism (pale skin, hair, and eye color).Alternative NamesKlein-Waardenburg syndrome; Waardenburg-Shah syndromeCauses, incidence, and risk factorsWaardenburg syndrome is inherited as an autosomal dominant trait, meaning only one parent has to pass on the faulty gene for a child to be affected.There are four main types of Waardenburg syndrome.The most common types are Type I and Type II.Type III (Klein-Waardenburg syndrome) and type IV (Waardenburg-Shah syndrome) are more rare.The multiple types of this syndrome result from mutations occurring in different genes. All types share two main features: hearing loss and pigment (color) changes in the skin, hair, and eyes. A white patch of hair may appear in an otherwise dark head of hair. Eyes may be very pale light-blue or each a different color.People with Type I may almost always have wide-set eyes. Hearing loss occurs more often in people with Type II than Type I.The less common types of this disease may cause problems with the arms or intestines.Almost 90% of people with this disease have a parent with the disease, but the symptoms in the parent can be quite different from those in the child.SymptomsCleft lip (rare)ConstipationDeafnessExtremely pale blue eyes or eye colors that don't match (heterochromia)Possible difficulty with completely straightening joints (contracture)Possible slight decrease in intellectual functionWhite patch of hair or early graying of the hairSigns and testsTests may include:AudiometryBowel transit timeColon biopsyGenetic testingTreatmentNo specific treatment is available for Waardenburg syndrome. Attention must be paid to any hearing deficits, and hearing aids and appropriate schooling may be needed. Special diets and medicines to keep the bowel moving are prescribed to type IV patients who have constipation.Expectations (prognosis)Once hearing problems are corrected, most people with this syndrome should be able to lead a normal life. Those with rarer forms of the syndrome may have additional problems, however, which can lead to complications.ComplicationsConstipation severe enough to require part of large bowel to be removedHearing lossSelf-esteem problems, or other problems related to appearanceSlight decreased intellectual functioning (possible, unusual)Slight increased risk for muscle tumor called rhabdomyosarcomaCalling your health care providerGenetic counseling may be helpful if you have family history of Waardenburg syndrome and plan to have children. Call for a hearing test if you or your child has deafness or decreased hearing.PreventionGenetic counseling may be valuable for prospective parents with a family history of Waardenburg syndrome.ReferencesMorelli JG. Hypopigmented Lesions. In: Kliegman RM, Behrman RE, Jenson HB, Stanton BF, eds. Nelson Textbook of Pediatrics. 18th Ed. Philadelphia, Pa: Saunders Elsevier; 2007: chap 652.
What human disease is caused by non-disjunction?
Down's syndrome is the most common.
What is the most common form of nerve entrapment?
The most common entrapment syndrome is carpal tunnel syndrome . Cubital tunnel syndrome of the ulnar nerve, which runs down the arm and through the elbow, also occurs frequently.
How common is marfan syndrome?
Marfan's syndrome is the most common genetic disorder of connective tissue. It occurs in about every 10,000 to 20,000 individuals.
The most common autosomal abnormality is seen is a person with?
Down syndrome
What is the most common cause for down syndrome?
Down's syndrome is a disorder caused by defective genes. It is most commonly caused by parents who are elderly at the time of birth.
Is down syndrome more common in certain populations?
it is the most popler up your but
