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Erschienen in: Journal of Inherited Metabolic Disease 2/2011

01.04.2011 | GALACTOSEMIA

Cross-sectional analysis of speech and cognitive performance in 32 patients with classic galactosemia

verfasst von: Björn Hoffmann, Udo Wendel, Susanne Schweitzer-Krantz

Erschienen in: Journal of Inherited Metabolic Disease | Ausgabe 2/2011

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Abstract

Background

Long-term outcome in classic galactosemia is disappointing with impaired IQ, reduced bone mineral density, and fertility problems. Moreover, speech impairment is common with conflicting reports regarding frequency, pattern, and relation to IQ.

Objective

To evaluate speech and cognitive performance in patients with galactosemia.

Methods

Speech performance was evaluated by means of the Hierarchische Wortlisten, a German word-repetition test for the diagnosis of apraxia of speech, using real words and pseudo-words. Cognitive performance was evaluated by use of age-appropriate German versions of the Wechsler Scales.

Results

In a cohort of 32 patients (12 females, 20 males; mean age 21.2 ± 7.2 years) with classic galactosemia, the mean IQ was 76.2 ± 14.8. Eighty-four percent of the patients passed the speech test with errors. Speech errors were much more related to pseudo-words than real words and were predominantly observed in words with three and four syllables. The performance in producing words was correlated to the IQ scores.

Conclusion

Impairment of speech affects a significant number of patients with galactosemia, appears in early childhood, and persists into adulthood. The pattern of speech impairment may allow labeling as apraxia of speech. In many cases impaired speech is related to decreased IQ.
Literatur
Zurück zum Zitat Ad Hoc Committee on Childhood Apraxia of Speech of the American Speech-Language-Hearing Association (2007) Childhood apraxia of speech: position statement. American Speech-Language-Hearing Association, Rockville, MD Ad Hoc Committee on Childhood Apraxia of Speech of the American Speech-Language-Hearing Association (2007) Childhood apraxia of speech: position statement. American Speech-Language-Hearing Association, Rockville, MD
Zurück zum Zitat Antshel KM, Epstein IO, Waisbren SE (2004) Cognitive strengths and weaknesses in children and adolescents homozygous for the galactosemia Q188R mutation: a descriptive study. Neuropsychology 18:658–664PubMedCrossRef Antshel KM, Epstein IO, Waisbren SE (2004) Cognitive strengths and weaknesses in children and adolescents homozygous for the galactosemia Q188R mutation: a descriptive study. Neuropsychology 18:658–664PubMedCrossRef
Zurück zum Zitat Badawi N, Cahalane SF, McDonald M, Mulhair P, Begi B, O'Donohue A, Naughten E (1996) Galactosaemia—a controversial disorder. Screening & outcome. Ireland 1972–1992. Ir Med J 89:16–17PubMed Badawi N, Cahalane SF, McDonald M, Mulhair P, Begi B, O'Donohue A, Naughten E (1996) Galactosaemia—a controversial disorder. Screening & outcome. Ireland 1972–1992. Ir Med J 89:16–17PubMed
Zurück zum Zitat Fishler K, Koch R, Donnell GN, Wenz E (1980) Developmental aspects of galactosemia from infancy to childhood. Clin Pediatr 19:38–44CrossRef Fishler K, Koch R, Donnell GN, Wenz E (1980) Developmental aspects of galactosemia from infancy to childhood. Clin Pediatr 19:38–44CrossRef
Zurück zum Zitat Flynn JR (1987) Massive IQ gains in 14 nations: what IQ tests really measure. Psychol Bull 101:171–191CrossRef Flynn JR (1987) Massive IQ gains in 14 nations: what IQ tests really measure. Psychol Bull 101:171–191CrossRef
Zurück zum Zitat Forges T, Monnier-Barbarino P, Leheup B, Jouvet P (2006) Pathophysiology of impaired ovarian function in galactosaemia. Hum Reprod Update 12:573–584PubMedCrossRef Forges T, Monnier-Barbarino P, Leheup B, Jouvet P (2006) Pathophysiology of impaired ovarian function in galactosaemia. Hum Reprod Update 12:573–584PubMedCrossRef
Zurück zum Zitat Friedman JH, Levy HL, Boustany RM (1989) Late onset of distinct neurologic syndromes in galactosemic siblings. Neurology 39:741–742PubMed Friedman JH, Levy HL, Boustany RM (1989) Late onset of distinct neurologic syndromes in galactosemic siblings. Neurology 39:741–742PubMed
Zurück zum Zitat Hansen TW, Henrichsen B, Rasmussen RK, Carling A, Andressen AB, Skjeldal O (1996) Neuropsychological and linguistic follow-up studies of children with galactosaemia from an unscreened population. Acta Paediatr 85:1197–1201PubMedCrossRef Hansen TW, Henrichsen B, Rasmussen RK, Carling A, Andressen AB, Skjeldal O (1996) Neuropsychological and linguistic follow-up studies of children with galactosaemia from an unscreened population. Acta Paediatr 85:1197–1201PubMedCrossRef
Zurück zum Zitat Jan JE, Wilson RA (1973) Unusual late neurological sequelae in galactosaemia. Dev Med Child Neurol 15:72–74PubMedCrossRef Jan JE, Wilson RA (1973) Unusual late neurological sequelae in galactosaemia. Dev Med Child Neurol 15:72–74PubMedCrossRef
Zurück zum Zitat Kaufman F, Kogut MD, Donnell GN, Koch H, Goebelsmann U (1979) Ovarian failure in galactosaemia. Lancet 2:737–738PubMedCrossRef Kaufman F, Kogut MD, Donnell GN, Koch H, Goebelsmann U (1979) Ovarian failure in galactosaemia. Lancet 2:737–738PubMedCrossRef
Zurück zum Zitat Kaufman FR, Reichardt JK, Ng WG et al (1994) Correlation of cognitive, neurologic, and ovarian outcome with the Q188R mutation of the galactose-1-phosphate uridyltransferase gene. J Pediatr 125:225–227PubMedCrossRef Kaufman FR, Reichardt JK, Ng WG et al (1994) Correlation of cognitive, neurologic, and ovarian outcome with the Q188R mutation of the galactose-1-phosphate uridyltransferase gene. J Pediatr 125:225–227PubMedCrossRef
Zurück zum Zitat Kaufman FR, McBride-Chang C, Manis FR, Wolff JA, Nelson MD (1995) Cognitive functioning, neurologic status and brain imaging in classical galactosemia. Eur J Pediatr 154:S2–S5PubMedCrossRef Kaufman FR, McBride-Chang C, Manis FR, Wolff JA, Nelson MD (1995) Cognitive functioning, neurologic status and brain imaging in classical galactosemia. Eur J Pediatr 154:S2–S5PubMedCrossRef
Zurück zum Zitat Koch TK, Schmidt KA, Wagstaff JE, Ng WG, Packman S (1992) Neurologic complications in galactosemia. Pediatr Neurol 8:217–220PubMedCrossRef Koch TK, Schmidt KA, Wagstaff JE, Ng WG, Packman S (1992) Neurologic complications in galactosemia. Pediatr Neurol 8:217–220PubMedCrossRef
Zurück zum Zitat Liepold M (1998) Hierarchische Wortlisten. Ein Nachsprechtest für die Sprechdiagnostik. Verlag Modernes Lernen, Dortmund Liepold M (1998) Hierarchische Wortlisten. Ein Nachsprechtest für die Sprechdiagnostik. Verlag Modernes Lernen, Dortmund
Zurück zum Zitat Liu G, Hale GE, Hughes CL (2000) Galactose metabolism and ovarian toxicity. Reprod Toxicol 14:377–384PubMedCrossRef Liu G, Hale GE, Hughes CL (2000) Galactose metabolism and ovarian toxicity. Reprod Toxicol 14:377–384PubMedCrossRef
Zurück zum Zitat Manis FR, Cohn LB, McBride-Chang C, Wolff JA, Kaufman FR (1997) A longitudinal study of cognitive functioning in patients with classical galactosaemia, including a cohort treated with oral uridine. J Inherit Metab Dis 20:549–555PubMedCrossRef Manis FR, Cohn LB, McBride-Chang C, Wolff JA, Kaufman FR (1997) A longitudinal study of cognitive functioning in patients with classical galactosaemia, including a cohort treated with oral uridine. J Inherit Metab Dis 20:549–555PubMedCrossRef
Zurück zum Zitat Nelson CD, Waggoner DD, Donnell GN, Tuerck JM, Buist NR (1991) Verbal dyspraxia in treated galactosemia. Pediatrics 88:346–350PubMed Nelson CD, Waggoner DD, Donnell GN, Tuerck JM, Buist NR (1991) Verbal dyspraxia in treated galactosemia. Pediatrics 88:346–350PubMed
Zurück zum Zitat Panis B, Forget PP, Van Kroonenburgh MJ et al (2004) Bone metabolism in galactosemia. Bone 35:982–987PubMedCrossRef Panis B, Forget PP, Van Kroonenburgh MJ et al (2004) Bone metabolism in galactosemia. Bone 35:982–987PubMedCrossRef
Zurück zum Zitat Potter NL, Lazarus JA, Johnson JM, Steiner RD, Shriberg LD (2008) Correlates of language impairment in children with galactosaemia. J Inherit Metab Dis 31:524–532PubMedCrossRef Potter NL, Lazarus JA, Johnson JM, Steiner RD, Shriberg LD (2008) Correlates of language impairment in children with galactosaemia. J Inherit Metab Dis 31:524–532PubMedCrossRef
Zurück zum Zitat Robertson A, Singh RH (2000) Outcomes analysis of verbal dyspraxia in classic galactosemia. Genet Med 2:142–148PubMedCrossRef Robertson A, Singh RH (2000) Outcomes analysis of verbal dyspraxia in classic galactosemia. Genet Med 2:142–148PubMedCrossRef
Zurück zum Zitat Satzger W, Dragon E, Engel R (1996) Zur Normäquivalenz von HAWIE-R und HAWIE. Diagnostica 43:119–138 Satzger W, Dragon E, Engel R (1996) Zur Normäquivalenz von HAWIE-R und HAWIE. Diagnostica 43:119–138
Zurück zum Zitat Schadewaldt P, Hoffmann B, Hammen HW, Kamp G, Schweitzer-Krantz S, Wendel U (2010) Longitudinal assessment of intellectual achievement in patients with classical galactosaemia. Pediatrics 125:e374–e381PubMedCrossRef Schadewaldt P, Hoffmann B, Hammen HW, Kamp G, Schweitzer-Krantz S, Wendel U (2010) Longitudinal assessment of intellectual achievement in patients with classical galactosaemia. Pediatrics 125:e374–e381PubMedCrossRef
Zurück zum Zitat Schallberger U (1987) HAWIK und HAWIK-R: ein empirischer Vergleich. Diagnostica 33:1–13 Schallberger U (1987) HAWIK und HAWIK-R: ein empirischer Vergleich. Diagnostica 33:1–13
Zurück zum Zitat Scheibenreiter S, Knoll E, Widhalm K (1992) Long-term results in children with classical galactosemia. Wien Klin Wochenschr 104:514–517PubMed Scheibenreiter S, Knoll E, Widhalm K (1992) Long-term results in children with classical galactosemia. Wien Klin Wochenschr 104:514–517PubMed
Zurück zum Zitat Schweitzer S, Shin Y, Jakobs C, Brodehl J (1993) Long-term outcome in 134 patients with galactosaemia. Eur J Pediatr 152:36–43PubMedCrossRef Schweitzer S, Shin Y, Jakobs C, Brodehl J (1993) Long-term outcome in 134 patients with galactosaemia. Eur J Pediatr 152:36–43PubMedCrossRef
Zurück zum Zitat Shield JP, Wadsworth EJ, MacDonald A et al (2000) The relationship of genotype to cognitive outcome in galactosaemia. Arch Dis Child 83:248–250PubMedCrossRef Shield JP, Wadsworth EJ, MacDonald A et al (2000) The relationship of genotype to cognitive outcome in galactosaemia. Arch Dis Child 83:248–250PubMedCrossRef
Zurück zum Zitat Shriberg LD, Aram DM, Kwiatkowski J (1997) Developmental apraxia of speech: I. descriptive and theoretical perspectives. J Speech Lang Hear Res 40:273–285PubMed Shriberg LD, Aram DM, Kwiatkowski J (1997) Developmental apraxia of speech: I. descriptive and theoretical perspectives. J Speech Lang Hear Res 40:273–285PubMed
Zurück zum Zitat Smith I, Beasley MG, Ades AE (1990) Intelligence and quality of dietary treatment in phenylketonuria. Arch Dis Child 65:472–478PubMedCrossRef Smith I, Beasley MG, Ades AE (1990) Intelligence and quality of dietary treatment in phenylketonuria. Arch Dis Child 65:472–478PubMedCrossRef
Zurück zum Zitat Waggoner DD, Buist NR, Donnell GN (1990) Long-term prognosis in galactosaemia: results of a survey of 350 cases. J Inherit Metab Dis 13:802–818PubMedCrossRef Waggoner DD, Buist NR, Donnell GN (1990) Long-term prognosis in galactosaemia: results of a survey of 350 cases. J Inherit Metab Dis 13:802–818PubMedCrossRef
Zurück zum Zitat Waisbren SE, Norman TR, Schnell RR, Levy HL (1983) Speech and language deficits in early-treated children with galactosemia. J Pediatr 102:75–77PubMedCrossRef Waisbren SE, Norman TR, Schnell RR, Levy HL (1983) Speech and language deficits in early-treated children with galactosemia. J Pediatr 102:75–77PubMedCrossRef
Zurück zum Zitat Webb AL, Singh RH, Kennedy MJ, Elsas LJ (2003) Verbal dyspraxia and galactosemia. Pediatr Res 53:396–402PubMedCrossRef Webb AL, Singh RH, Kennedy MJ, Elsas LJ (2003) Verbal dyspraxia and galactosemia. Pediatr Res 53:396–402PubMedCrossRef
Metadaten
Titel
Cross-sectional analysis of speech and cognitive performance in 32 patients with classic galactosemia
verfasst von
Björn Hoffmann
Udo Wendel
Susanne Schweitzer-Krantz
Publikationsdatum
01.04.2011
Verlag
Springer Netherlands
Erschienen in
Journal of Inherited Metabolic Disease / Ausgabe 2/2011
Print ISSN: 0141-8955
Elektronische ISSN: 1573-2665
DOI
https://doi.org/10.1007/s10545-011-9297-5

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