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Marshall syndrome was named after Dr. John Marshall, who first described the condition in the medical literature. The syndrome is characterized by features such as skeletal abnormalities, facial dysmorphism, and hearing loss. Naming it after Dr. Marshall honors his contributions to understanding and identifying the disorder, which is a form of connective tissue disorder.
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Who is Tourette syndrome named for?
The disorder is named for another French physician, Georges Gilles de la Tourette
Who is Jacobs syndrome named after?
Jacobs syndrome is named after Dr. D. H. Jacobs, who first described the condition in 1961. It is a genetic disorder resulting from the presence of an extra Y chromosome in males, leading to a 47, XYY karyotype. Individuals with Jacobs syndrome may exhibit certain physical and behavioral characteristics, although many lead typical lives.
Did john langdon really discover down syndrome?
His name is John Langdon Down. The disorder was named after him.
Why is 'Down syndrome' spelled with a capital 'D'?
Down syndrome starts with a capital letter because it is named after John Langdon Down, the doctor who described the disorder in 1866.
What type of genetic disorder is waardenburg syndrome?
Waardenburg synrome is an autosomal genetic disorder characterized by deafness, confluent brows, early grey hair as young as 12, different colored eyes or unusually brilliant blue eyes. Source US NIH Deafness and other communcation disorders. Its named Waardenburg because it was discovered Prietrus Waardenburg who noticed girls and boys with unmatching eyes tend to deafness. There are four main types.
How is any syndrome named?
Any syndrome named after its discoverer.
What is pfeiffer?
Pfeiffer syndrome is a genetic disorder characterized by the premature fusion of certain bones of the skull (craniosynostosis), which prevents further growth of the skull and affects the shape of the head and face. In addition, the thumbs and big toes are broader and often shorter than normal. It is named for Rudolf Arthur Pfeiffer.Pfeiffer syndrome affects about 1 in 100,000 individuals.For the source and more detailed information concerning this request, click on the related links section (Answers.com) indicated below this answer box.Pfeiffer syndrome is a genetic disorder characterized by the premature fusion of certain bones of the skull (craniosynostosis), which prevents further growth of the skull and affects the shape of the head and face. In addition, the thumbs and big toes are broader and often shorter than normal. It is named for Rudolf Arthur Pfeiffer.Pfeiffer syndrome affects about 1 in 100,000 individuals.For the source and more detailed information concerning this request, click on the related links section (Answers.com) indicated below this answer box.Pfeiffer syndrome is a genetic disorder characterized by the premature fusion of certain bones of the skull (craniosynostosis), which prevents further growth of the skull and affects the shape of the head and face. In addition, the thumbs and big toes are broader and often shorter than normal. It is named for Rudolf Arthur Pfeiffer.Pfeiffer syndrome affects about 1 in 100,000 individuals.For the source and more detailed information concerning this request, click on the related links section (Answers.com) indicated below this answer box.Pfeiffer syndrome is a genetic disorder characterized by the premature fusion of certain bones of the skull (craniosynostosis), which prevents further growth of the skull and affects the shape of the head and face. In addition, the thumbs and big toes are broader and often shorter than normal. It is named for Rudolf Arthur Pfeiffer.Pfeiffer syndrome affects about 1 in 100,000 individuals.For the source and more detailed information concerning this request, click on the related links section (Answers.com) indicated below this answer box.Pfeiffer syndrome is a genetic disorder characterized by the premature fusion of certain bones of the skull (craniosynostosis), which prevents further growth of the skull and affects the shape of the head and face. In addition, the thumbs and big toes are broader and often shorter than normal. It is named for Rudolf Arthur Pfeiffer.Pfeiffer syndrome affects about 1 in 100,000 individuals.For the source and more detailed information concerning this request, click on the related links section (Answers.com) indicated below this answer box.Pfeiffer syndrome is a genetic disorder characterized by the premature fusion of certain bones of the skull (craniosynostosis), which prevents further growth of the skull and affects the shape of the head and face. In addition, the thumbs and big toes are broader and often shorter than normal. It is named for Rudolf Arthur Pfeiffer.Pfeiffer syndrome affects about 1 in 100,000 individuals.For the source and more detailed information concerning this request, click on the related links section (Answers.com) indicated below this answer box.
Who discovered Lesch-Nyhan syndrome?
Lesch-Nyhan syndrome was first described in 1964 by Drs. Michael Lesch and William Nyhan. The enzyme deficiency that causes the disorder was discovered in 1967 by a researcher named Seegmiller.
What is pfeiffers syndrome?
Pfeiffer syndrome is a genetic disorder characterized by the premature fusion of certain bones of the skull (craniosynostosis), which prevents further growth of the skull and affects the shape of the head and face. In addition, the thumbs and big toes are broader and often shorter than normal. It is named for Rudolf Arthur Pfeiffer.Pfeiffer syndrome affects about 1 in 100,000 individuals.For the source and more detailed information concerning this request, click on the related links section (Answers.com) indicated below this answer box.Pfeiffer syndrome is a genetic disorder characterized by the premature fusion of certain bones of the skull (craniosynostosis), which prevents further growth of the skull and affects the shape of the head and face. In addition, the thumbs and big toes are broader and often shorter than normal. It is named for Rudolf Arthur Pfeiffer.Pfeiffer syndrome affects about 1 in 100,000 individuals.For the source and more detailed information concerning this request, click on the related links section (Answers.com) indicated below this answer box.Pfeiffer syndrome is a genetic disorder characterized by the premature fusion of certain bones of the skull (craniosynostosis), which prevents further growth of the skull and affects the shape of the head and face. In addition, the thumbs and big toes are broader and often shorter than normal. It is named for Rudolf Arthur Pfeiffer.Pfeiffer syndrome affects about 1 in 100,000 individuals.For the source and more detailed information concerning this request, click on the related links section (Answers.com) indicated below this answer box.Pfeiffer syndrome is a genetic disorder characterized by the premature fusion of certain bones of the skull (craniosynostosis), which prevents further growth of the skull and affects the shape of the head and face. In addition, the thumbs and big toes are broader and often shorter than normal. It is named for Rudolf Arthur Pfeiffer.Pfeiffer syndrome affects about 1 in 100,000 individuals.For the source and more detailed information concerning this request, click on the related links section (Answers.com) indicated below this answer box.Pfeiffer syndrome is a genetic disorder characterized by the premature fusion of certain bones of the skull (craniosynostosis), which prevents further growth of the skull and affects the shape of the head and face. In addition, the thumbs and big toes are broader and often shorter than normal. It is named for Rudolf Arthur Pfeiffer.Pfeiffer syndrome affects about 1 in 100,000 individuals.For the source and more detailed information concerning this request, click on the related links section (Answers.com) indicated below this answer box.Pfeiffer syndrome is a genetic disorder characterized by the premature fusion of certain bones of the skull (craniosynostosis), which prevents further growth of the skull and affects the shape of the head and face. In addition, the thumbs and big toes are broader and often shorter than normal. It is named for Rudolf Arthur Pfeiffer.Pfeiffer syndrome affects about 1 in 100,000 individuals.For the source and more detailed information concerning this request, click on the related links section (Answers.com) indicated below this answer box.
Who is the Marshall Islands named after?
General Marshall
Which disorder affects the adrenal glands and can cause weakness cramps and convulsions?
Conn's syndrome is a condition affecting the adrenal glands that causes weakness, cramps, and convulsions. It was named after Jerome Conn, an American endocrinologist, who first described the disorder.
Who is Patau Syndrome named after?
Named for Dr. Klaus Patau, who reported the syndrome in 1960. It is sometimes called Bartholin-Patau syndrome, named in part for Thomas Bartholin, who described an infant with the syndrome in 1656.
