apnea has been researched along with Atrophy in 8 studies
Apnea: A transient absence of spontaneous respiration.
Atrophy: Decrease in the size of a cell, tissue, organ, or multiple organs, associated with a variety of pathological conditions such as abnormal cellular changes, ischemia, malnutrition, or hormonal changes.
| Excerpt | Relevance | Reference |
|---|---|---|
| " A symptom not described in PGAP1 related disorder before but prominent in the siblings were recurrent apnea especially during sleep that persisted at least until age 2 years." | 8.93 | Compound heterozygous variants in PGAP1 causing severe psychomotor retardation, brain atrophy, recurrent apneas and delayed myelination: a case report and literature review. ( Dreha-Kulaczewski, S; Elpeleg, O; Gärtner, J; Henneke, M; Huppke, P; Kettwig, M; Wegener, E, 2016) |
| "We report an 11-month-old boy with acetazolamide-responsive epileptic apnea and inherited glycosylphosphatidylinositol (GPI)-anchor deficiency who presented with decreased serum alkaline phosphatase associated with compound PIGT mutations." | 7.88 | Epileptic apnea in a patient with inherited glycosylphosphatidylinositol anchor deficiency and PIGT mutations. ( Adachi, Y; Ishiyama, A; Kinoshita, T; Kohashi, K; Matsumoto, N; Miya, K; Murakami, Y; Ohba, C; Saitsu, H; Sasaki, M; Sato, N; Sugai, K; Tanaka, T; Yuasa, S, 2018) |
| " A symptom not described in PGAP1 related disorder before but prominent in the siblings were recurrent apnea especially during sleep that persisted at least until age 2 years." | 4.93 | Compound heterozygous variants in PGAP1 causing severe psychomotor retardation, brain atrophy, recurrent apneas and delayed myelination: a case report and literature review. ( Dreha-Kulaczewski, S; Elpeleg, O; Gärtner, J; Henneke, M; Huppke, P; Kettwig, M; Wegener, E, 2016) |
| "We report an 11-month-old boy with acetazolamide-responsive epileptic apnea and inherited glycosylphosphatidylinositol (GPI)-anchor deficiency who presented with decreased serum alkaline phosphatase associated with compound PIGT mutations." | 3.88 | Epileptic apnea in a patient with inherited glycosylphosphatidylinositol anchor deficiency and PIGT mutations. ( Adachi, Y; Ishiyama, A; Kinoshita, T; Kohashi, K; Matsumoto, N; Miya, K; Murakami, Y; Ohba, C; Saitsu, H; Sasaki, M; Sato, N; Sugai, K; Tanaka, T; Yuasa, S, 2018) |
| "Brain abscess and hypoxemia were thought to be serious complications resulting from CAPV and were successfully corrected by living donor liver transplantation at the age of 4 months." | 1.33 | Successful liver transplantation for congenital absence of the portal vein complicated by intrapulmonary shunt and brain abscess. ( Doi, H; Haga, H; Kamei, H; Kasahara, M; Ogawa, K; Ogura, Y; Ohnishi, Y; Tanaka, K; Ueda, M; Yoshitoshi, EY, 2005) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (25.00) | 18.7374 |
| 1990's | 3 (37.50) | 18.2507 |
| 2000's | 1 (12.50) | 29.6817 |
| 2010's | 2 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kohashi, K | 1 |
| Ishiyama, A | 1 |
| Yuasa, S | 1 |
| Tanaka, T | 1 |
| Miya, K | 1 |
| Adachi, Y | 1 |
| Sato, N | 1 |
| Saitsu, H | 1 |
| Ohba, C | 1 |
| Matsumoto, N | 1 |
| Murakami, Y | 1 |
| Kinoshita, T | 1 |
| Sugai, K | 1 |
| Sasaki, M | 1 |
| Kettwig, M | 1 |
| Elpeleg, O | 1 |
| Wegener, E | 1 |
| Dreha-Kulaczewski, S | 1 |
| Henneke, M | 1 |
| Gärtner, J | 1 |
| Huppke, P | 1 |
| Ohnishi, Y | 1 |
| Ueda, M | 1 |
| Doi, H | 1 |
| Kasahara, M | 1 |
| Haga, H | 1 |
| Kamei, H | 1 |
| Ogawa, K | 1 |
| Ogura, Y | 1 |
| Yoshitoshi, EY | 1 |
| Tanaka, K | 1 |
| Ramelli, GP | 1 |
| Donati, F | 1 |
| Bianchetti, M | 1 |
| Vassella, F | 1 |
| Chokroverty, S | 1 |
| Sharp, JT | 1 |
| Barron, KD | 1 |
| Helbing, WA | 1 |
| van der Blij, JF | 1 |
| ten Houten, R | 1 |
| Broere, G | 1 |
| Oorthuys, JW | 1 |
| Pérez-Garrigues, H | 1 |
| Burguera, JA | 1 |
| López Arlandis Gea, A | 1 |
| De Souza, SW | 1 |
| Davis, JA | 1 |
1 review available for apnea and Atrophy
| Article | Year |
|---|---|
Compound heterozygous variants in PGAP1 causing severe psychomotor retardation, brain atrophy, recurrent apneas and delayed myelination: a case report and literature review.
Topics: Apnea; Atrophy; Brain; Brain Diseases; Child, Preschool; Developmental Disabilities; Humans; Magneti | 2016 |
7 other studies available for apnea and Atrophy
| Article | Year |
|---|---|
Epileptic apnea in a patient with inherited glycosylphosphatidylinositol anchor deficiency and PIGT mutations.
Topics: Abnormalities, Multiple; Acyltransferases; Apnea; Atrophy; Developmental Disabilities; Epilepsy; Gly | 2018 |
Successful liver transplantation for congenital absence of the portal vein complicated by intrapulmonary shunt and brain abscess.
Topics: Abnormalities, Multiple; Anti-Bacterial Agents; Apnea; Atrophy; Birth Weight; Brain; Brain Abscess; | 2005 |
Apnoeic attacks as an isolated manifestation of epileptic seizures in infants.
Topics: Apnea; Atrophy; Diagnosis, Differential; Electroencephalography; Epilepsy; Female; Frontal Lobe; Hea | 1998 |
Periodic respiration in erect posture in Shy-Drager syndrome.
Topics: Apnea; Atrophy; Cerebellum; Electrocardiography; Electroencephalography; Electromyography; Gliosis; | 1978 |
[Attacks of apnea in an infant with achondroplasia].
Topics: Achondroplasia; Apnea; Atrophy; Brain; Female; Humans; Infant; Life Expectancy; Magnetic Resonance I | 1991 |
[Laryngeal stridor caused by Gerhardt's syndrome in olivopontocerebellar atrophy and a probable striatonigral degeneration].
Topics: Apnea; Atrophy; Corpus Striatum; Female; Humans; Middle Aged; Olivopontocerebellar Atrophies; Respir | 1990 |
Spinal cord damage in a newborn infant.
Topics: Apnea; Atrophy; Birth Injuries; Birth Weight; Cephalometry; Cyanosis; Female; Fetal Heart; Heart Rat | 1974 |