Page last updated: 2024-10-31

apnea and Fragile X Syndrome

apnea has been researched along with Fragile X Syndrome in 1 studies

Apnea: A transient absence of spontaneous respiration.

Fragile X Syndrome: A condition characterized genotypically by mutation of the distal end of the long arm of the X chromosome (at gene loci FRAXA or FRAXE) and phenotypically by cognitive impairment, hyperactivity, SEIZURES, language delay, and enlargement of the ears, head, and testes. INTELLECTUAL DISABILITY occurs in nearly all males and roughly 50% of females with the full mutation of FRAXA. (From Menkes, Textbook of Child Neurology, 5th ed, p226)

Research Excerpts

ExcerptRelevanceReference
" This was followed by apnea associated with cyanosis and oxygen desaturation."3.73Cyanotic episodes in a male child with fragile X syndrome. ( Herzog, K; Kothare, SV; Miller-Horn, J, 2006)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Miller-Horn, J1
Herzog, K1
Kothare, SV1

Other Studies

1 other study available for apnea and Fragile X Syndrome

ArticleYear
Cyanotic episodes in a male child with fragile X syndrome.
    Developmental medicine and child neurology, 2006, Volume: 48, Issue:8

    Topics: Apnea; Behavior Therapy; Child; Cyanosis; Fragile X Syndrome; Humans; Hyperventilation; Male; Self-I

2006