Laryngeal abductor paralysis




Input patient's signs and symptoms


Narrow down the case reports



Total: 14 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
1
(4.0%)
22579632
Bilateral vocal cord abductor paralysis associated with primary herpes simplex infection: a case report.
Dupuch V, Saroul N, Aumeran C, Pastourel R, Mom T, Gilain L.
Eur Ann Otorhinolaryngol Head Neck Dis. 2012;129(5):272-4.
Dysphonia
Antiviral Agents Follow-Up Studies Homo sapiens Intravenous Injections Male Middle Aged Time Factors Vocal Cord Paralysis
1
(4.0%)
17826894
Assessment of autonomic dysfunction of multiple system atrophy with laryngeal abductor paralysis as an early manifestation.
Deguchi K, Ikeda K, Shimamura M, Urai Y, Tsukaguchi M, Touge T, Takeuchi H, Sasaki I, Kuriyama S.
Clin Neurol Neurosurg. 2007;109(10):892-5.
Orthostatic hypotension
Cerebellar Ataxia Differential Diagnosis Females Homo sapiens Human Growth Hormone Male Middle Aged Multiple System Atrophy Neurologic Examination Shy-Drager Syndrome Vocal Cord Paralysis
1
(4.0%)
11715334
[Autonomic dysfunction with nocturnal dyspnea (Gerhardt-syndrome) in a patient with multiple system atrophy].
Eissler M, Holocher R, Lindenstrauss M, Wild K, Braun B.
Med Klin (Munich). 2001;96(10):626-31.
Syncope
Differential Diagnosis Dyspnea Homo sapiens Male Middle Aged Multiple System Atrophy Olivopontocerebellar Atrophies Respiratory Sounds Shy-Drager Syndrome Syncope Syndrome
1
(4.0%)
11376202
Adult-onset familial laryngeal abductor paralysis, cerebellar ataxia, and pure motor neuropathy.
Barbieri F, Pellecchia MT, Esposito E, Di Stasio E, Castaldo I, Santorelli F, Perretti A, Santoro L, De Michele G.
Neurology. 2001;56(10):1412-4.
Ataxia
Cerebellum Homo sapiens Magnetic Resonance Imaging Male Middle Aged Motor Neuron Disease Peripheral Nervous System Diseases Spinocerebellar Degeneration Vocal Cord Paralysis Voice Disorders
1
(4.0%)
10349349
[Effective nasal CPAP therapy for heavy snoring and paradoxical respiration during sleep in a case of multiple system atrophy].
Miyamoto M, Miyamoto T, Katayama S, Hirata K.
Rinsho Shinkeigaku. 1998;38(12):1059-63.
Ataxia
CENPJ
Homo sapiens Male Middle Aged Multiple System Atrophy Positive-Pressure Respiration Sleep Apnea Syndromes Snoring
1
(4.0%)
9600735
Familial laryngeal paralysis.
Manaligod JM, Smith RJ.
Am J Med Genet. 1998;77(4):277-80.
Paralysis
Females Homo sapiens Infant Male Vocal Cord Paralysis
1
(4.0%)
7958087
[A case of Shy-Drager syndrome complicated with syndrome of inappropriate secretion of antidiuretic hormone (SIADH) and incomplete paralysis of bilateral vocal cords].
Sone H, Okuda Y, Bannai C, Asano M, Asakura Y, Yamaoka T, Suzuki S, Kawakami Y, Odawara M, Matsushima T, et al..
Nihon Naibunpi Gakkai Zasshi. 1994;70(2):75-84.
Urinary incontinence
Homo sapiens Inappropriate ADH Syndrome Male Shy-Drager Syndrome Vocal Cord Paralysis
1
(4.0%)
7718959
Syndrome of inappropriate secretion of antidiuretic hormone (SIADH) and Gerhardt syndrome associated with Shy-Drager syndrome.
Sone H, Okuda Y, Bannai C, Suzuki S, Yamaoka T, Asakura Y, Kawakami Y, Odawara M, Matsushima T, Kawai K, et al..
Intern Med. 1994;33(12):773-8.
Hyponatremia
Homo sapiens Inappropriate ADH Syndrome Male Shy-Drager Syndrome Vocal Cord Paralysis
1
(4.0%)
7237099
Laryngeal abductor paralysis in multiple system atrophy. A report on three necropsied cases, with observations on the laryngeal muscles and the nuclei ambigui.
Bannister R, Gibson W, Michaels L, Oppenheimer DR.
Brain. 1981;104(2):351-68.
Paralysis
Brain Homo sapiens Larynx Male Medulla Oblongata Middle Aged Shy-Drager Syndrome Vocal Cord Paralysis
1
(4.0%)
4058983
Familial vocal cord dysfunction.
Cunningham MJ, Eavey RD, Shannon DC.
Pediatrics. 1985;76(5):750-3.
Vocal cord paralysis
Airway Obstruction Females Homo sapiens Infant, Newborn Male Respiratory Function Tests Respiratory Sounds Vocal Cord Paralysis
        

Phenotype(s) retrieved from Orphanet

    Total: 2

HPO ID Term Frequency
HP:0001601 Laryngomalacia Very frequent (99-80%)
HP:0002093 Respiratory insufficiency Frequent (79-30%)


Phenotype(s) retrieved from case reports

    Total: 6

HPO ID Term # of case reports
HP:0003470 Paralysis 3
HP:0001251 Ataxia 1
HP:0001605 Vocal cord paralysis 1
HP:0001618 Dysphonia 1
HP:0002094 Dyspnea 1
HP:0010535 Sleep apnea 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID