Page last updated: 2024-10-31

apnea and Atrophy

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.

Research Excerpts

ExcerptRelevanceReference
" 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."8.93Compound 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."7.88Epileptic 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."4.93Compound 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."3.88Epileptic 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."1.33Successful 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)

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19902 (25.00)18.7374
1990's3 (37.50)18.2507
2000's1 (12.50)29.6817
2010's2 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Kohashi, K1
Ishiyama, A1
Yuasa, S1
Tanaka, T1
Miya, K1
Adachi, Y1
Sato, N1
Saitsu, H1
Ohba, C1
Matsumoto, N1
Murakami, Y1
Kinoshita, T1
Sugai, K1
Sasaki, M1
Kettwig, M1
Elpeleg, O1
Wegener, E1
Dreha-Kulaczewski, S1
Henneke, M1
Gärtner, J1
Huppke, P1
Ohnishi, Y1
Ueda, M1
Doi, H1
Kasahara, M1
Haga, H1
Kamei, H1
Ogawa, K1
Ogura, Y1
Yoshitoshi, EY1
Tanaka, K1
Ramelli, GP1
Donati, F1
Bianchetti, M1
Vassella, F1
Chokroverty, S1
Sharp, JT1
Barron, KD1
Helbing, WA1
van der Blij, JF1
ten Houten, R1
Broere, G1
Oorthuys, JW1
Pérez-Garrigues, H1
Burguera, JA1
López Arlandis Gea, A1
De Souza, SW1
Davis, JA1

Reviews

1 review available for apnea and Atrophy

ArticleYear
Compound heterozygous variants in PGAP1 causing severe psychomotor retardation, brain atrophy, recurrent apneas and delayed myelination: a case report and literature review.
    BMC neurology, 2016, May-21, Volume: 16

    Topics: Apnea; Atrophy; Brain; Brain Diseases; Child, Preschool; Developmental Disabilities; Humans; Magneti

2016

Other Studies

7 other studies available for apnea and Atrophy

ArticleYear
Epileptic apnea in a patient with inherited glycosylphosphatidylinositol anchor deficiency and PIGT mutations.
    Brain & development, 2018, Volume: 40, Issue:1

    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.
    Journal of pediatric surgery, 2005, Volume: 40, Issue:5

    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.
    European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society, 1998, Volume: 2, Issue:4

    Topics: Apnea; Atrophy; Diagnosis, Differential; Electroencephalography; Epilepsy; Female; Frontal Lobe; Hea

1998
Periodic respiration in erect posture in Shy-Drager syndrome.
    Journal of neurology, neurosurgery, and psychiatry, 1978, Volume: 41, Issue:11

    Topics: Apnea; Atrophy; Cerebellum; Electrocardiography; Electroencephalography; Electromyography; Gliosis;

1978
[Attacks of apnea in an infant with achondroplasia].
    Tijdschrift voor kindergeneeskunde, 1991, Volume: 59, Issue:3

    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].
    Anales otorrinolaringologicos ibero-americanos, 1990, Volume: 17, Issue:1

    Topics: Apnea; Atrophy; Corpus Striatum; Female; Humans; Middle Aged; Olivopontocerebellar Atrophies; Respir

1990
Spinal cord damage in a newborn infant.
    Archives of disease in childhood, 1974, Volume: 49, Issue:1

    Topics: Apnea; Atrophy; Birth Injuries; Birth Weight; Cephalometry; Cyanosis; Female; Fetal Heart; Heart Rat

1974