Cafe-au-Lait Spots

"Cafe-au-Lait Spots" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

Light brown pigmented macules associated with NEUROFIBROMATOSIS and Albright's syndrome (see FIBROUS DYSPLASIA, POLYOSTOTIC).

Descriptor ID

D019080

MeSH Number(s)

C17.800.621.250

C23.888.885.250

Concept/Terms

Cafe-au-Lait Spots

Below are MeSH descriptors whose meaning is more general than "Cafe-au-Lait Spots".

Diseases [C]
Skin and Connective Tissue Diseases [C17]
Skin Diseases [C17.800]
Pigmentation Disorders [C17.800.621]
Cafe-au-Lait Spots [C17.800.621.250]
Pathological Conditions, Signs and Symptoms [C23]
Signs and Symptoms [C23.888]
Skin Manifestations [C23.888.885]
Cafe-au-Lait Spots [C23.888.885.250]

Below are MeSH descriptors whose meaning is related to "Cafe-au-Lait Spots".

Below are MeSH descriptors whose meaning is more specific than "Cafe-au-Lait Spots".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Cafe-au-Lait Spots" by people in Harvard Catalyst Profiles by year, and whether "Cafe-au-Lait Spots" was a major or minor topic of these publication.

Below are the most recent publications written about "Cafe-au-Lait Spots" by people in Profiles.

Implications of mosaicism in variant interpretation: A case of a de novo homozygous NF1 variant. Eur J Med Genet. 2021 Jul; 64(7):104236.

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Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation. Genet Med. 2021 08; 23(8):1506-1513.

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Cancer and constitutional Mismatch Repair Deficiency syndrome due to homozygous MSH 6 mutation in children with Café au Lait Spots and review of literature. Turk J Pediatr. 2021; 63(5):893-902.

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Café au lait spots: When and how to pursue their genetic origins. Clin Dermatol. 2020 Jul - Aug; 38(4):421-431.

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A 15-Month-Old Girl Presenting With Clitoromegaly and a Chest Mass. Semin Pediatr Neurol. 2018 07; 26:128-131.

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Jaffe-Campanacci syndrome, revisited: detailed clinical and molecular analyses determine whether patients have neurofibromatosis type 1, coincidental manifestations, or a distinct disorder. Genet Med. 2014 Jun; 16(6):448-59.

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Can the diagnosis of NF1 be excluded clinically? A lack of pigmentary findings in families with spinal neurofibromatosis demonstrates a limitation of clinical diagnosis. J Med Genet. 2013 Sep; 50(9):606-13.

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JAAD Grand Rounds quiz. Café-au-lait macules and enlarging papules on the face. J Am Acad Dermatol. 2013 Feb; 68(2):348-50.

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SPRED proteins provide a NF-ty link to Ras suppression. Genes Dev. 2012 Jul 15; 26(14):1515-9.

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Incidence of Fanconi anemia in children with congenital thumb anomalies referred for diepoxybutane testing. J Hand Surg Am. 2011 Jun; 36(6):1052-7.

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