Multiple café au lait spots in familial patients with MAP2K2 mutation

Toshiki Takenouchi, Atsushi Shimizu, Chiharu Torii, Rika Kosaki, Takao Takahashi, Hideyuki Saya, Kenjiro Kosaki

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

Recent advances in genetic diagnostic technologies have made the classic disease nosology highly complicated. This situation is exemplified by rasopathies, among which neurofibromatosis type 1 and Noonan syndrome represent prototypic entities. The former condition is characterized by multiple café au lait spots and neurofibromas, while the latter is characterized by distinct facial features, webbed neck, congenital heart disease, and a short stature. On rare occasions, the features of both neurofibromatosis and Noonan syndrome co-exist within an individual; such patients are diagnosed as having neurofibromatosis-Noonan syndrome. Here, we report familial patients with multiple café au lait spots and Noonan syndrome-like facial features. A mutation analysis unexpectedly revealed a mutation in MAP2K2 in both the propositus and his mother. The propositus fulfilled the diagnostic criteria for neurofibromatosis type 1, but his mother did not. Their phenotype was not consistent with that of cardio-facio-cutaneous syndrome, which is classically known to be associated with MAP2K2 mutations. The mother of the propositus had cervical cancer at the age of 23 years, consistent with the oncogenic tendency associated with rasopathies. The phenotypic combination of multiple café au lait spots and Noonan syndrome-like facial features suggested a diagnosis of neurofibromatosis-Noonan syndrome. Whether this condition represents a discrete disease entity or a variable expression of neurofibromatosis type 1 has long been debated. The present observation suggests that some perturbation in the RAS/MAPK signaling cascade results in multiple café au lait spots, a key diagnostic phenotype of rasopathies, although the exact mechanism remains to be elucidated.

Original languageEnglish
Pages (from-to)392-396
Number of pages5
JournalAmerican Journal of Medical Genetics, Part A
Volume164
Issue number2
DOIs
Publication statusPublished - 2014 Feb

Fingerprint

Neurofibromatosis 1
Mutation
Mothers
Phenotype
Neurofibroma
Uterine Cervical Neoplasms
Heart Diseases
Neck
Technology
Neurofibromatosis-Noonan syndrome
Noonan like syndrome

Keywords

  • Cafe au lait spots
  • MAP2K2
  • Neurofibromatosis type 1
  • Neurofibromatosis-Noonan syndrome
  • Noonan syndrome
  • Rasopathies

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics

Cite this

Multiple café au lait spots in familial patients with MAP2K2 mutation. / Takenouchi, Toshiki; Shimizu, Atsushi; Torii, Chiharu; Kosaki, Rika; Takahashi, Takao; Saya, Hideyuki; Kosaki, Kenjiro.

In: American Journal of Medical Genetics, Part A, Vol. 164, No. 2, 02.2014, p. 392-396.

Research output: Contribution to journalArticle

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