Pallister-Hall syndrome is a rare inherited disorder that affects several body systems at once. Its two defining features are a non-cancerous mass on the hypothalamus, called a hypothalamic hamartoma, and extra fingers or toes, with the skin between some digits sometimes fused. The hamartoma may cause no trouble, but in some people it leads to seizures, classically brief laughing or gelastic seizures, or to hormone abnormalities. Other features can include a split in the airway, a blocked anal opening and kidney abnormalities, and severity ranges from mild to severe. The condition is caused by a shortened, altered GLI3 gene and passes in an autosomal dominant pattern, though some cases arise from new mutations. It was first described by the geneticists Philip Pallister and Judith Hall, and about one hundred cases have been reported in the literature.
Facts
Classification
ICD-10 ChapterIII: Diseases of the Blood and Blood-Forming Organs and Certain Disorders Involving the Immune Mechanism 2 Communicable or Non-communicable Transmission Route Causative Agent
Causative Agent (category) Prevalence Band Sources
1. Pallister-Hall syndrome (Wikipedia)
Lead sentence
The main features are a non-cancerous mass on the hypothalamus (hypothalamic hamartoma) and extra digits (polydactylism).
Transmission section
Pallister-Hall Syndrome occurs due to a mutation in the GLI3 gene that overrides normal genetic development.
View the Source2. Orphadata (Orphanet): Orphadata cross-references for ORPHA:672 Pallister-Hall syndrome
Orphadata (Orphanet)ICD-10 cross-referenceQuote, ICD-10 cross-reference
"Reference": "D33.0", "Source": "ICD-10"
View the Source 3. National Cancer Institute (NCI Thesaurus): Pallister-Hall syndrome - NCI Thesaurus concept C84987
National Cancer Institute (NCI Thesaurus)DefinitionQuote, Definition
A very rare autosomal dominant inherited disorder caused by mutations in the GLI3 gene.
View the Source 4. MedlinePlus Genetics (U.S. National Library of Medicine): Pallister-Hall syndrome - MedlinePlus Genetics
MedlinePlus Genetics (U.S. National Library of Medicine)Description and InheritanceQuote, Description and Inheritance
Mutations in the GLI3 gene cause Pallister-Hall syndrome.
View the Source 5. Orphadata (Orphanet): Orphadata: Epidemiology of rare diseases (en_product9_prev)
Orphadata (Orphanet)ORPHA:672Quote, ORPHA:672
Point prevalence Class only <1 / 1 000 000
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