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Meralgia paraesthetica, familial

MedGen UID:: 322555
•Concept ID:: C1835026
•: Disease or Syndrome

Synonym:	Meralgia Paraesthetica, Familial

Monarch Initiative:	MONDO:0007975
OMIM®:	156220

Clinical features

From HPO

Abnormality of the nervous system

MedGen UID:: 105425
•Concept ID:: C0497552
•: Congenital Abnormality

An abnormality of the nervous system.

See: Feature record | Search on this feature

Abnormality of the nervous system
- Abnormality of the nervous system

Recent clinical studies

Diagnosis

Nerve entrapment syndromes in dermatology: Review and practical approach to treatment.

Zagarella S
Australas J Dermatol 2018 Nov;59(4):286-290. Epub 2018 Apr 20 doi: 10.1111/ajd.12822. PMID: 29676437

Meralgia paresthetica: 3-Tesla magnetic resonance neurography.

Chhabra A, Del Grande F, Soldatos T, Chalian M, Belzberg AJ, Williams EH, Jalali FS, Thawait GK, Eng J, Carrino JA
Skeletal Radiol 2013 Jun;42(6):803-8. Epub 2013 Jan 11 doi: 10.1007/s00256-012-1557-4. PMID: 23306718

Prognosis

Meralgia paresthetica: 3-Tesla magnetic resonance neurography.

Chhabra A, Del Grande F, Soldatos T, Chalian M, Belzberg AJ, Williams EH, Jalali FS, Thawait GK, Eng J, Carrino JA
Skeletal Radiol 2013 Jun;42(6):803-8. Epub 2013 Jan 11 doi: 10.1007/s00256-012-1557-4. PMID: 23306718

Clinical prediction guides

Meralgia paresthetica: 3-Tesla magnetic resonance neurography.

Chhabra A, Del Grande F, Soldatos T, Chalian M, Belzberg AJ, Williams EH, Jalali FS, Thawait GK, Eng J, Carrino JA
Skeletal Radiol 2013 Jun;42(6):803-8. Epub 2013 Jan 11 doi: 10.1007/s00256-012-1557-4. PMID: 23306718

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Coriell Institute for Medical Research

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Meralgia paraesthetica, familial
Meralgia paraesthetica, familial

MedGen
inter-alpha-trypsin inhibitor heavy chain H5 isoform X1 [Homo sapiens]
inter-alpha-trypsin inhibitor heavy chain H5 isoform X1 [Homo sapiens]
gi|2462521198|ref|XP_054222814.1|

Protein
Homo sapiens
Homo sapiens
RefSeq annotation of the human reference genome assembly

BioProject
BioProject Links for Nucleotide (Select 2217354067) (1)
BioProject
Neurodevelopmental disorder with relative macrocephaly and with or without cardi...
Neurodevelopmental disorder with relative macrocephaly and with or without cardiac or endocrine anomalies

MedGen

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