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Pallister-Hall syndrome

Congenital Malformations and Chromosomal Abnormalities

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
Body System
Nervous System 1
ICD-10 Chapter
III: Diseases of the Blood and Blood-Forming Organs and Certain Disorders Involving the Immune Mechanism 2
Communicable or Non-communicable
Non-Communicable 3
Transmission Route
Non-Transmissible 4
Causative Agent
Causative Agent (category)
Genetic / Hereditary 1
Prevalence Band
Rare (Under 1 in 2000) 5
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.
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2. Orphadata (Orphanet): Orphadata cross-references for ORPHA:672 Pallister-Hall syndrome
Orphadata (Orphanet)ICD-10 cross-reference
Quote, ICD-10 cross-reference
"Reference": "D33.0", "Source": "ICD-10"
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3. National Cancer Institute (NCI Thesaurus): Pallister-Hall syndrome - NCI Thesaurus concept C84987
National Cancer Institute (NCI Thesaurus)Definition
Quote, Definition
A very rare autosomal dominant inherited disorder caused by mutations in the GLI3 gene.
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4. MedlinePlus Genetics (U.S. National Library of Medicine): Pallister-Hall syndrome - MedlinePlus Genetics
MedlinePlus Genetics (U.S. National Library of Medicine)Description and Inheritance
Quote, Description and Inheritance
Mutations in the GLI3 gene cause Pallister-Hall syndrome.
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5. Orphadata (Orphanet): Orphadata: Epidemiology of rare diseases (en_product9_prev)
Orphadata (Orphanet)ORPHA:672
Quote, ORPHA:672
Point prevalence Class only <1 / 1 000 000
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