apnea has been researched along with Sick Sinus Node Syndrome in 2 studies
Apnea: A transient absence of spontaneous respiration.
| Excerpt | Relevance | Reference |
|---|---|---|
| " He developed severe apnea, epilepsy, and psychomotor developmental delay and died suddenly of sick sinus syndrome at 17 months of age." | 7.88 | MECP2 mutation in a boy with severe apnea and sick sinus syndrome. ( Fukuoka, T; Kaname, T; Shioda, T; Takahashi, S; Yamauchi, T, 2018) |
| " Two males and one female had intellectual disability and apnea, but none met the criteria of Rett syndrome." | 3.96 | Two males with sick sinus syndrome in a family with 0.6 kb deletions involving major domains in MECP2. ( Endo, W; Haginoya, K; Inui, T; Iwama, K; Kakisaka, Y; Kikuchi, A; Kure, S; Matsumoto, N; Miyabayashi, T; Mizuguchi, T; Okubo, Y; Sato, R; Togashi, N, 2020) |
| " He developed severe apnea, epilepsy, and psychomotor developmental delay and died suddenly of sick sinus syndrome at 17 months of age." | 3.88 | MECP2 mutation in a boy with severe apnea and sick sinus syndrome. ( Fukuoka, T; Kaname, T; Shioda, T; Takahashi, S; Yamauchi, T, 2018) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 1 (50.00) | 2.80 |
| Authors | Studies |
|---|---|
| Inui, T | 1 |
| Iwama, K | 1 |
| Miyabayashi, T | 1 |
| Sato, R | 1 |
| Okubo, Y | 1 |
| Endo, W | 1 |
| Togashi, N | 1 |
| Kakisaka, Y | 1 |
| Kikuchi, A | 1 |
| Mizuguchi, T | 1 |
| Kure, S | 1 |
| Matsumoto, N | 1 |
| Haginoya, K | 1 |
| Shioda, T | 1 |
| Takahashi, S | 1 |
| Kaname, T | 1 |
| Yamauchi, T | 1 |
| Fukuoka, T | 1 |
2 other studies available for apnea and Sick Sinus Node Syndrome
| Article | Year |
|---|---|
Two males with sick sinus syndrome in a family with 0.6 kb deletions involving major domains in MECP2.
Topics: Apnea; Autonomic Nervous System Diseases; Child; Child, Preschool; Chromosomes, Human, X; Exome Sequ | 2020 |
MECP2 mutation in a boy with severe apnea and sick sinus syndrome.
Topics: Apnea; Child, Preschool; Fatal Outcome; Humans; Infant; Male; Methyl-CpG-Binding Protein 2; Mutation | 2018 |