Skip to main content
Erschienen in: Current Neurology and Neuroscience Reports 6/2013

01.06.2013 | Neuro-ophthalmology (A Kawasaki, Section Editor)

Fourth Cranial Nerve Palsy and Brown Syndrome: Two Interrelated Congenital Cranial Dysinnervation Disorders?

Erschienen in: Current Neurology and Neuroscience Reports | Ausgabe 6/2013

Einloggen, um Zugang zu erhalten

Abstract

Based on neuroimaging data showing absence of the trochlear nerve, congenital superior oblique palsy is now classified as a congenital cranial dysinnervation disorder. A similar absence of the abducens nerve is accompanied by misinnervation to the lateral rectus muscle from a branch of oculomotor nerve in the Duane retraction syndrome. This similarity raises the question of whether some cases of Brown syndrome could arise from a similar synkinesis between the inferior and superior oblique muscles in the setting of congenital superior oblique palsy. This hypothesis has gained support from the confluence of evidence from a number of independent studies. Using Duane syndrome as a model, we critically review the accumulating evidence that some cases of Brown syndrome are ultimately attributable to dysgenesis of the trochlear nerve.
Literatur
1.
Zurück zum Zitat Brown HW. Congenital structural muscle anomalies. In: Allen J, editor. Strabismus ophthalmic symposium. St Louis, MO: C.V. Mosby; 1950. p. 205–36. Brown HW. Congenital structural muscle anomalies. In: Allen J, editor. Strabismus ophthalmic symposium. St Louis, MO: C.V. Mosby; 1950. p. 205–36.
2.
Zurück zum Zitat Harley RD, Rodrigues MM, Crawford JS. Congenital fibrosis of the extraocular muscles. Trans Am Ophthalmol Soc. 1978;76:197–226.PubMed Harley RD, Rodrigues MM, Crawford JS. Congenital fibrosis of the extraocular muscles. Trans Am Ophthalmol Soc. 1978;76:197–226.PubMed
3.
Zurück zum Zitat Brodsky MC. Hereditary external ophthalmoplegia synergistic divergence, jaw winking, and oculocutaneous hypopigmentation: a congenital fibrosis syndrome caused by deficient innervation to extraocular muscles. Ophthalmology. 1998;105:717–25.PubMedCrossRef Brodsky MC. Hereditary external ophthalmoplegia synergistic divergence, jaw winking, and oculocutaneous hypopigmentation: a congenital fibrosis syndrome caused by deficient innervation to extraocular muscles. Ophthalmology. 1998;105:717–25.PubMedCrossRef
4.
Zurück zum Zitat Brodsky MC. The doctor's eye: seeing through the myopathy of congenital ptosis. Ophthalmology. 2000;107:1973–4.PubMedCrossRef Brodsky MC. The doctor's eye: seeing through the myopathy of congenital ptosis. Ophthalmology. 2000;107:1973–4.PubMedCrossRef
5.
Zurück zum Zitat Gutowski NJ, Bosley TM, Engle EC. The congenital cranial dysinnervation disorders. Neuromuscul Disord. 2003;13:573–8.PubMedCrossRef Gutowski NJ, Bosley TM, Engle EC. The congenital cranial dysinnervation disorders. Neuromuscul Disord. 2003;13:573–8.PubMedCrossRef
6.
Zurück zum Zitat Traboulsi EI. Congenital cranial dysinnervation disorders and more. J AAPOS. 2007;11:215–7.PubMedCrossRef Traboulsi EI. Congenital cranial dysinnervation disorders and more. J AAPOS. 2007;11:215–7.PubMedCrossRef
7.
Zurück zum Zitat Pieh C, Lagrèze WA. Congenital cranial dysinnervation disorders. Ophthalmology. 2007;104:1083–95.CrossRef Pieh C, Lagrèze WA. Congenital cranial dysinnervation disorders. Ophthalmology. 2007;104:1083–95.CrossRef
8.
Zurück zum Zitat • Neugebauer A, Fricke J. Congenital cranial dysinnervation disorders: facts and perspectives to understand ocular motility disorders. In: Lorenz B, Brodsky MC, editors. Essentials in ophthalmology:pPediatric ophthalmology, neuro-ophthalmology, genetics. Berlin, Heidelberg: Springer-Verlag; 2010. p. 83–7. The authors present both theoretical arguments and critical analysis of a large series of 87 cases of congenital Brown syndrome leading to consider congenital Brown syndrome as a CCDD. • Neugebauer A, Fricke J. Congenital cranial dysinnervation disorders: facts and perspectives to understand ocular motility disorders. In: Lorenz B, Brodsky MC, editors. Essentials in ophthalmology:pPediatric ophthalmology, neuro-ophthalmology, genetics. Berlin, Heidelberg: Springer-Verlag; 2010. p. 83–7. The authors present both theoretical arguments and critical analysis of a large series of 87 cases of congenital Brown syndrome leading to consider congenital Brown syndrome as a CCDD.
9.
Zurück zum Zitat Oystreck DT, Engle EC, Bosley TM. Recent progress in understanding congenital cranial dysinnervation disorders. J Neuro-Ophthalmol. 2011;31:69–77.CrossRef Oystreck DT, Engle EC, Bosley TM. Recent progress in understanding congenital cranial dysinnervation disorders. J Neuro-Ophthalmol. 2011;31:69–77.CrossRef
10.
Zurück zum Zitat Assaf AA. Congenital innervation dysgenesis syndrome (CID)/congenital cranial dysinnervation disorders (CCDDs). Eye. 2011;25:1251–61.PubMedCrossRef Assaf AA. Congenital innervation dysgenesis syndrome (CID)/congenital cranial dysinnervation disorders (CCDDs). Eye. 2011;25:1251–61.PubMedCrossRef
11.
Zurück zum Zitat Brodsky MC. Ocular motor nerve palsies in children. In: Pediatric neuro-ophthalmology. 2nd ed. New York: Springer; 2010. p. 253–308.CrossRef Brodsky MC. Ocular motor nerve palsies in children. In: Pediatric neuro-ophthalmology. 2nd ed. New York: Springer; 2010. p. 253–308.CrossRef
12.
Zurück zum Zitat Yüksel D, de Xivry JJ O, Lefèvre P. Review of the major findings about Duane retraction syndrome (DRS) leading to an update form of classification. Vision Res. 2010;50:2334–47.PubMedCrossRef Yüksel D, de Xivry JJ O, Lefèvre P. Review of the major findings about Duane retraction syndrome (DRS) leading to an update form of classification. Vision Res. 2010;50:2334–47.PubMedCrossRef
13.
Zurück zum Zitat Heuck G. Über angeborenen vererbeten Beweglichkeitsdefect der Augent. Klin Monatsbl Augenheilkd. 1879;17:253. Heuck G. Über angeborenen vererbeten Beweglichkeitsdefect der Augent. Klin Monatsbl Augenheilkd. 1879;17:253.
14.
Zurück zum Zitat Bielschowsky A. Lectures on motor anomalies. Hanover, NH: Dartmouth College Publications; 1943/1956. Bielschowsky A. Lectures on motor anomalies. Hanover, NH: Dartmouth College Publications; 1943/1956.
15.
Zurück zum Zitat Türk S. Bemerkungen zu einem Fall von Retraktion des Auges. Centralbl Pract Augenheilkd. 1899;23:14. Türk S. Bemerkungen zu einem Fall von Retraktion des Auges. Centralbl Pract Augenheilkd. 1899;23:14.
16.
Zurück zum Zitat Hoyt WF, Nachtigaller H. Anomalies of ocular motor nerves: neuroanatomic correlates of paradoxical innervation in Duane’s syndrome and related congenital ocular motor disorder. Am J Ophthalmol. 1965;60:443–8.PubMed Hoyt WF, Nachtigaller H. Anomalies of ocular motor nerves: neuroanatomic correlates of paradoxical innervation in Duane’s syndrome and related congenital ocular motor disorder. Am J Ophthalmol. 1965;60:443–8.PubMed
17.
Zurück zum Zitat Breinin GM. Electromyography: a tool in ocular and neurologic diagnosis. II. Muscle palsy. Arch Ophthalmol. 1957;57:165–75.CrossRef Breinin GM. Electromyography: a tool in ocular and neurologic diagnosis. II. Muscle palsy. Arch Ophthalmol. 1957;57:165–75.CrossRef
18.
Zurück zum Zitat Matteuci P. I difetti congenti di abduzione con particolare riguardo alla pathogenesis. Rassegna Ital Ottalmologia. 1946;15:345–80. Matteuci P. I difetti congenti di abduzione con particolare riguardo alla pathogenesis. Rassegna Ital Ottalmologia. 1946;15:345–80.
19.
Zurück zum Zitat Hotchkiss MG, Miller NR, Clark AW, Green WR. Bilateral Duane’s retraction syndrome. A clinical-pathologic case report. Arch Ophthalmol. 1980;98:870–4.PubMedCrossRef Hotchkiss MG, Miller NR, Clark AW, Green WR. Bilateral Duane’s retraction syndrome. A clinical-pathologic case report. Arch Ophthalmol. 1980;98:870–4.PubMedCrossRef
20.
Zurück zum Zitat Miller NR, Kiel SM, Green WR, et al. Unilateral Duane’s retraction syndrome (TypI). Arch Ophthalmol. 1982;00:1468–72.CrossRef Miller NR, Kiel SM, Green WR, et al. Unilateral Duane’s retraction syndrome (TypI). Arch Ophthalmol. 1982;00:1468–72.CrossRef
21.
Zurück zum Zitat • Robert MP, Parsa CF. Thromboembolism and congenital malformations: from Duane syndrome to Thalidomide embryopathy. Arch Ophthalmol. 2012;10:1–9. The authors propose that thromboembolism and focal cerebral hypoperfusion could cause Duane retraction syndrome and other congenital malformations, as an alternative to genetic mutations.CrossRef • Robert MP, Parsa CF. Thromboembolism and congenital malformations: from Duane syndrome to Thalidomide embryopathy. Arch Ophthalmol. 2012;10:1–9. The authors propose that thromboembolism and focal cerebral hypoperfusion could cause Duane retraction syndrome and other congenital malformations, as an alternative to genetic mutations.CrossRef
22.
Zurück zum Zitat Kang NY, Demer JL. Comparison of orbital magnetic resonance imaging in Duane syndrome and abducens palsy. Am J Ophthalmol. 2006;142:827–34.PubMedCrossRef Kang NY, Demer JL. Comparison of orbital magnetic resonance imaging in Duane syndrome and abducens palsy. Am J Ophthalmol. 2006;142:827–34.PubMedCrossRef
23.
Zurück zum Zitat Parsa CF, Grant E, Dillon WP, du Lac S, Hoyt WF. Absence of the abducens nerve in Duane syndrome verified by magnetic resonance imaging. Am J Ophthalmol. 1998;125:399–401.PubMedCrossRef Parsa CF, Grant E, Dillon WP, du Lac S, Hoyt WF. Absence of the abducens nerve in Duane syndrome verified by magnetic resonance imaging. Am J Ophthalmol. 1998;125:399–401.PubMedCrossRef
24.
Zurück zum Zitat Oskurt H, Basak M, Oral Y, et al. Magnetic resonance imaging in Duane’s retraction syndrome. J Pediatr Ophthalmol Strabismus. 2003;40:19–22. Oskurt H, Basak M, Oral Y, et al. Magnetic resonance imaging in Duane’s retraction syndrome. J Pediatr Ophthalmol Strabismus. 2003;40:19–22.
25.
Zurück zum Zitat Kim HJ, Hwang JM. Presence of the abducens nerve according to the type of Duane’s retraction syndrome. Ophthalmology. 2005;112:109–13.PubMedCrossRef Kim HJ, Hwang JM. Presence of the abducens nerve according to the type of Duane’s retraction syndrome. Ophthalmology. 2005;112:109–13.PubMedCrossRef
26.
Zurück zum Zitat Demer JL, Clark RA, Lim DK, Engle EC. Magnetic resonance imaging evidence for widespread orbital dysinnervation in dominang Duane’s retraction syndrome linked to DURS2 locus. Invest Ophthalmol Vis Sci. 2007;48:194–202.PubMedCrossRef Demer JL, Clark RA, Lim DK, Engle EC. Magnetic resonance imaging evidence for widespread orbital dysinnervation in dominang Duane’s retraction syndrome linked to DURS2 locus. Invest Ophthalmol Vis Sci. 2007;48:194–202.PubMedCrossRef
27.
Zurück zum Zitat Demer JL, Clark RA, Lim DK, Engle EC. Magnetic resonance imaging of innervational and extraocular muscle abnormalities in Duane-radial-ray syndrome. Invest Ophthalmol Vis Sci. 2007;48:5505–11.PubMedCrossRef Demer JL, Clark RA, Lim DK, Engle EC. Magnetic resonance imaging of innervational and extraocular muscle abnormalities in Duane-radial-ray syndrome. Invest Ophthalmol Vis Sci. 2007;48:5505–11.PubMedCrossRef
28.
Zurück zum Zitat Holmes JM, Mutyala S, Mous TL, et al. Pediatric third, fourth, and sixth nerve palsies: a population-based study. Am J Opthtalmol. 1999;127:388–92.CrossRef Holmes JM, Mutyala S, Mous TL, et al. Pediatric third, fourth, and sixth nerve palsies: a population-based study. Am J Opthtalmol. 1999;127:388–92.CrossRef
29.
Zurück zum Zitat Kolling GH. Diagnostik und operative Korrektur von Vertikal- und Zyklodeviationen bei Störungen schräger Augenmuskeln. Dosis-Wirkungsbeziehung verschiedener Eingriffe. Giessen: Habilitationsschrift; 1986. Kolling GH. Diagnostik und operative Korrektur von Vertikal- und Zyklodeviationen bei Störungen schräger Augenmuskeln. Dosis-Wirkungsbeziehung verschiedener Eingriffe. Giessen: Habilitationsschrift; 1986.
30.
Zurück zum Zitat Steffen J, Kolling GH. Heterotopie. In: Kaufman H, Steffen H, editors. Strabismus. 4th ed. Stuttgart: Thieme; 2012. p. 247. Steffen J, Kolling GH. Heterotopie. In: Kaufman H, Steffen H, editors. Strabismus. 4th ed. Stuttgart: Thieme; 2012. p. 247.
31.
Zurück zum Zitat von Noorden GK, Murray E, Wong SY. Superior oblique paralysis. A review of 270 cases. Arch Ophthalmol. 1986;104:1771–6.CrossRef von Noorden GK, Murray E, Wong SY. Superior oblique paralysis. A review of 270 cases. Arch Ophthalmol. 1986;104:1771–6.CrossRef
32.
Zurück zum Zitat Mottier ME, Mets MB. Vertical fusional vergences in patients with superior oblique palsies. Am Orthopt J. 1990;40:88–93. Mottier ME, Mets MB. Vertical fusional vergences in patients with superior oblique palsies. Am Orthopt J. 1990;40:88–93.
33.
Zurück zum Zitat Wallace DK, von Noorden GK. Clinical characteristics and surgical management of congenital absence of the superior oblique tendon. Am J Ophthalmol. 1994;118:63–9.PubMed Wallace DK, von Noorden GK. Clinical characteristics and surgical management of congenital absence of the superior oblique tendon. Am J Ophthalmol. 1994;118:63–9.PubMed
34.
Zurück zum Zitat Helveston EM, Krach D, Plager DA, Ellis FD. A new classification of superior oblique palsy based on congenital variations in the tendon. Ophthalmology. 1992;99:1609.PubMed Helveston EM, Krach D, Plager DA, Ellis FD. A new classification of superior oblique palsy based on congenital variations in the tendon. Ophthalmology. 1992;99:1609.PubMed
35.
Zurück zum Zitat Plager DA. Traction testing in superior oblique palsy. J Pediatr Ophthalmol Strabismsus. 1990;27:136. Plager DA. Traction testing in superior oblique palsy. J Pediatr Ophthalmol Strabismsus. 1990;27:136.
36.
Zurück zum Zitat Plager DA. Tendon laxity in superior oblique palsy. Ophthalmology. 1992;99:1032.PubMed Plager DA. Tendon laxity in superior oblique palsy. Ophthalmology. 1992;99:1032.PubMed
37.
Zurück zum Zitat Sato M. Magnetic resonance imaging and tendon anomaly associated with congenital superior oblique palsy. Am J Ophthalmol. 1999;127:379.PubMedCrossRef Sato M. Magnetic resonance imaging and tendon anomaly associated with congenital superior oblique palsy. Am J Ophthalmol. 1999;127:379.PubMedCrossRef
38.
Zurück zum Zitat Sato M, Yagasaki T, Kora T, Awaya S. Comparison of muscle volume between congenital and acquired superior oblique palsies by magnetic resonance imaging. Jpn J Ophthalmol. 1998;42:466.PubMedCrossRef Sato M, Yagasaki T, Kora T, Awaya S. Comparison of muscle volume between congenital and acquired superior oblique palsies by magnetic resonance imaging. Jpn J Ophthalmol. 1998;42:466.PubMedCrossRef
39.
Zurück zum Zitat Clark RA, Miller JM, Rosenbaum AL, Demer JL. Heterotopic rectus muscle pulleys or oblique muscle dysfunctionl. J AAPOS. 1998;2:17–25.PubMedCrossRef Clark RA, Miller JM, Rosenbaum AL, Demer JL. Heterotopic rectus muscle pulleys or oblique muscle dysfunctionl. J AAPOS. 1998;2:17–25.PubMedCrossRef
40.
Zurück zum Zitat Jiang Y, Matsuo T, Fujiwara H, et al. ARIX gene polymorphisms in patients with congenital superior oblique muscle palsy. Br J Ophthalmol. 2004;88:263–7.PubMedCrossRef Jiang Y, Matsuo T, Fujiwara H, et al. ARIX gene polymorphisms in patients with congenital superior oblique muscle palsy. Br J Ophthalmol. 2004;88:263–7.PubMedCrossRef
41.
Zurück zum Zitat Traboulsi EI. Congenital abnormalities of cranial nerve development: overview, molecular mechanisms, and further evidence of heterogeneity and complexity of syndromes with congenital limitation of eye movements. Trans Am Ophthalmol Soc. 2004;102:373–89.PubMed Traboulsi EI. Congenital abnormalities of cranial nerve development: overview, molecular mechanisms, and further evidence of heterogeneity and complexity of syndromes with congenital limitation of eye movements. Trans Am Ophthalmol Soc. 2004;102:373–89.PubMed
42.
Zurück zum Zitat •• Kim JH, Hwang JM. Absence of the trochlear nerve in patients with superior oblique hypoplasia. Ophthalmology. 2010;117:2208–13. The authors used a very high-resolution cranial nerve MRI technique allowing visualization of the trochlear nerve in 100% of cases to show that the trochlear nerve was absent in patients with superior oblique hypoplasia. Based on that observation, they suggested that congenital superior oblique palsy with superior oblique hypoplasia should be classified as a CCDD.PubMedCrossRef •• Kim JH, Hwang JM. Absence of the trochlear nerve in patients with superior oblique hypoplasia. Ophthalmology. 2010;117:2208–13. The authors used a very high-resolution cranial nerve MRI technique allowing visualization of the trochlear nerve in 100% of cases to show that the trochlear nerve was absent in patients with superior oblique hypoplasia. Based on that observation, they suggested that congenital superior oblique palsy with superior oblique hypoplasia should be classified as a CCDD.PubMedCrossRef
43.
Zurück zum Zitat •• Yang HK, Kim JH, Hwang JM. Congenital superior oblique palsy and trochlear nerve absence. A clinical and radiological study. Ophthalmology. 2012;119:170–7. In this study, a large series of 97 consecutive patients diagnosed with congenital superior oblique palsy were studied with cerebral MRI to evaluate the presence of the trochlear nerve. The trochlear nerve was absent on the affected side in 73% of cases, consistent with a CCDD.PubMedCrossRef •• Yang HK, Kim JH, Hwang JM. Congenital superior oblique palsy and trochlear nerve absence. A clinical and radiological study. Ophthalmology. 2012;119:170–7. In this study, a large series of 97 consecutive patients diagnosed with congenital superior oblique palsy were studied with cerebral MRI to evaluate the presence of the trochlear nerve. The trochlear nerve was absent on the affected side in 73% of cases, consistent with a CCDD.PubMedCrossRef
44.
Zurück zum Zitat Parks MM, Brown M. Superior oblique tendon sheath syndrome of Brown. Am J Ophthalmol. 1975;79:82–6.PubMed Parks MM, Brown M. Superior oblique tendon sheath syndrome of Brown. Am J Ophthalmol. 1975;79:82–6.PubMed
45.
46.
Zurück zum Zitat Papst W, Stein HJ. Etiology of the superior oblique tendon sheath syndrome. Klin Monatsbl Augenheilkd. 1969;154:506–18.PubMed Papst W, Stein HJ. Etiology of the superior oblique tendon sheath syndrome. Klin Monatsbl Augenheilkd. 1969;154:506–18.PubMed
47.
Zurück zum Zitat Ferig-Seiwerth F, Celic M. A contribution to the knowledge of superior oblique tendon sheath syndrome (Brown’s syndrome). Orthoptics. Proceedings of the Second International Orthoptic Congress, Amsterdam, May 11–13. Excerpta Medica. 1971;1972:354–9. Ferig-Seiwerth F, Celic M. A contribution to the knowledge of superior oblique tendon sheath syndrome (Brown’s syndrome). Orthoptics. Proceedings of the Second International Orthoptic Congress, Amsterdam, May 11–13. Excerpta Medica. 1971;1972:354–9.
48.
Zurück zum Zitat Kolling G, Rohde S, Kress B. Congenital Brown’s syndrome is caused by missing fourth cranial nerve in some cases. Presented at the 32nd Meeting of the European Strabismological Association, Munich, Germany, September 7–10, 2008. Kolling G, Rohde S, Kress B. Congenital Brown’s syndrome is caused by missing fourth cranial nerve in some cases. Presented at the 32nd Meeting of the European Strabismological Association, Munich, Germany, September 7–10, 2008.
49.
Zurück zum Zitat • Kaeser PF, Kress B, Rohde S, Kolling G. Absence of the fourth cranial nerve in congenital Brown syndrome. Acta Ophthalmol. 2012;90:e310–3. In this study, MR imaging showed that trochlear nerve was absent in 2 patients with congenital Brown syndrome, while superior oblique muscle was normal in size (ie, not hypoplastic) and did not relax as it should in upgaze. This study adds an anatomical support to consider some cases of congenital Brown syndrome as CCDD.PubMedCrossRef • Kaeser PF, Kress B, Rohde S, Kolling G. Absence of the fourth cranial nerve in congenital Brown syndrome. Acta Ophthalmol. 2012;90:e310–3. In this study, MR imaging showed that trochlear nerve was absent in 2 patients with congenital Brown syndrome, while superior oblique muscle was normal in size (ie, not hypoplastic) and did not relax as it should in upgaze. This study adds an anatomical support to consider some cases of congenital Brown syndrome as CCDD.PubMedCrossRef
50.
Zurück zum Zitat • Ellis FJ, Jeffery AR, Seidman DJ, Sprague JB, Coussens T, Schuller J. Possible association of congenital Brown syndrome with congenital cranial dysinnervation disorders. J AAPOS. 2012;16:558–64. The authors propose that congenital superior oblique palsy and Brown syndrome could both be secondary to an abnormal development of the trochlear nerve resulting in secondary physical changes of the superior oblique muscle, tendon, or trochlea.PubMedCrossRef • Ellis FJ, Jeffery AR, Seidman DJ, Sprague JB, Coussens T, Schuller J. Possible association of congenital Brown syndrome with congenital cranial dysinnervation disorders. J AAPOS. 2012;16:558–64. The authors propose that congenital superior oblique palsy and Brown syndrome could both be secondary to an abnormal development of the trochlear nerve resulting in secondary physical changes of the superior oblique muscle, tendon, or trochlea.PubMedCrossRef
51.
Zurück zum Zitat Dawson E, Barry J, Lee J. Spontaneous resolution in patients with congenital Brown syndrome. J AAPOS. 2009;13:116–8.PubMedCrossRef Dawson E, Barry J, Lee J. Spontaneous resolution in patients with congenital Brown syndrome. J AAPOS. 2009;13:116–8.PubMedCrossRef
52.
Zurück zum Zitat Kaeser PF, Maeder P, Klainguti G. Absence of the fourth cranial nerve in persistent congenital Brown syndrome [poster POS2520]. 2nd World Congress of Pediatric Ophthalmology and Strabismus, Milano, Italy, September 7–9, 2012. Kaeser PF, Maeder P, Klainguti G. Absence of the fourth cranial nerve in persistent congenital Brown syndrome [poster POS2520]. 2nd World Congress of Pediatric Ophthalmology and Strabismus, Milano, Italy, September 7–9, 2012.
53.
Zurück zum Zitat Khan AO, Shinwari J, Al Sharif L, et al. Infantile esotropia could be oligogenic and allelic with Duane retraction syndrome. Mol Vis. 2011;17:1997–2002.PubMed Khan AO, Shinwari J, Al Sharif L, et al. Infantile esotropia could be oligogenic and allelic with Duane retraction syndrome. Mol Vis. 2011;17:1997–2002.PubMed
Metadaten
Titel
Fourth Cranial Nerve Palsy and Brown Syndrome: Two Interrelated Congenital Cranial Dysinnervation Disorders?
Publikationsdatum
01.06.2013
Erschienen in
Current Neurology and Neuroscience Reports / Ausgabe 6/2013
Print ISSN: 1528-4042
Elektronische ISSN: 1534-6293
DOI
https://doi.org/10.1007/s11910-013-0352-5

Weitere Artikel der Ausgabe 6/2013

Current Neurology and Neuroscience Reports 6/2013 Zur Ausgabe

Movement Disorders (SA Factor, Section Editor)

Freezing of Gait in Parkinson’s Disease: Where Are We Now?

Pediatric Neurology (D Nordli, Section Editor)

Diagnostic Criteria for Pediatric Multiple Sclerosis

Movement Disorders (SA Factor, Section Editor)

What is Essential Tremor?

Leitlinien kompakt für die Neurologie

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

„Restriktion auf vier Wochen Therapie bei Schlaflosigkeit ist absurd!“

06.05.2024 Insomnie Nachrichten

Chronische Insomnie als eigenständiges Krankheitsbild ernst nehmen und adäquat nach dem aktuellen Forschungsstand behandeln: Das forderte der Schlafmediziner Dr. Dieter Kunz von der Berliner Charité beim Praxis Update.

Stuhltransfusion könnte Fortschreiten von Parkinson-Symptomen bremsen

03.05.2024 Parkinson-Krankheit Nachrichten

Kann eine frühzeitige Stuhltransplantation das Fortschreiten von Parkinson-Symptomen verlangsamen? Die Ergebnisse einer randomisierten Phase-2-Studie scheinen dafür zu sprechen.

Frühe Tranexamsäure-Therapie nützt wenig bei Hirnblutungen

02.05.2024 Hirnblutung Nachrichten

Erhalten Personen mit einer spontanen Hirnblutung innerhalb von zwei Stunden nach Symptombeginn eine Tranexamsäure-Therapie, kann dies weder die Hämatomexpansion eindämmen noch die Mortalität senken.

Sind Frauen die fähigeren Ärzte?

30.04.2024 Gendermedizin Nachrichten

Patienten, die von Ärztinnen behandelt werden, dürfen offenbar auf bessere Therapieergebnisse hoffen als Patienten von Ärzten. Besonders scheint das auf weibliche Kranke zuzutreffen, wie eine Studie zeigt.

Update Neurologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.