Literature DB >> 1601004

Progressive high frequency hearing loss: an additional feature in the syndrome of congenital adrenal hypoplasia and gonadotrophin deficiency.

M Zachmann1, E Fuchs, A Prader.   

Abstract

In an earlier report, we found that X-linked congenital adrenal hypoplasia may be associated with gonadotrophin deficiency. This combination has since been confirmed by many others. At the last examination, our patients were 22.4, 19.9 and 17.5 years old. They were doing well on replacement therapy with hydrocortisone, fluorohydrocortisone, and long-acting testosterone, but in all of them, a progressive hearing loss had appeared, starting at high frequencies at about 14 years of age. The loss progressed with age to lower frequencies, and the oldest patient had some remaining hearing capacity at 125-500 Hz only with a perceptive hearing loss of -95 dB at frequencies above 500 Hz. It is concluded that patients with this syndrome should be examined for hearing loss. X-linked adrenal hypoplasia may also be associated with glycerol kinase deficiency and myopathy. A molecular XP-deletion has suggested a locus for hypogonadotrophic hypogonadism distal to the glycerol kinase and adrenal hypoplasia loci. The observations in our patients suggest that the locus for at least this type of X-linked deafness may be in the same area.

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Year:  1992        PMID: 1601004     DOI: 10.1007/bf01954375

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  21 in total

1.  Tables for predicting adult height from skeletal age: revised for use with the Greulich-Pyle hand standards.

Authors:  N BAYLEY; S R PINNEAU
Journal:  J Pediatr       Date:  1952-04       Impact factor: 4.406

2.  Familial congenital adrenal hypoplasia.

Authors:  C G Brook; M Bambach; M Zachmann; A Prader
Journal:  Helv Paediatr Acta       Date:  1973-10

3.  Congenital adrenal hypoplasia.

Authors:  N H Rasmussen; J Christoffersen; M Damkjaer Nielsen
Journal:  Acta Paediatr Scand       Date:  1986-09

4.  Concordance of X-linked glycerol kinase deficiency with X-linked congenital adrenal hypoplasia.

Authors:  J A Bartley; D K Miller; J T Hayford; E R McCabe
Journal:  Lancet       Date:  1982-10-02       Impact factor: 79.321

5.  Failure to induce puberty in a man with X-linked congenital adrenal hypoplasia and hypogonadotropic hypogonadism by pulsatile administration of low-dose gonadotropin-releasing hormone.

Authors:  K Kikuchi; M Kaji; T Momoi; H Mikawa; Y Shigematsu; M Sudo
Journal:  Acta Endocrinol (Copenh)       Date:  1987-01

6.  Contrasting effects of subcutaneous pulsatile GnRH therapy in congenital adrenal hypoplasia and Kallmann's syndrome.

Authors:  D Gordon; H N Cohen; G H Beastall; I D Hay; J A Thomson
Journal:  Clin Endocrinol (Oxf)       Date:  1984-12       Impact factor: 3.478

7.  Familial cytomegalic adrenocortical hypoplasia: an X-linked syndrome of pubertal failure.

Authors:  I D Hay; P J Smail; C C Forsyth
Journal:  Arch Dis Child       Date:  1981-09       Impact factor: 3.791

8.  Hypogonadism in congenital adrenal hypoplasia: evidence for a hypothalamic origin.

Authors:  K Kruse; W G Sippell; K V Schnakenburg
Journal:  J Clin Endocrinol Metab       Date:  1984-01       Impact factor: 5.958

9.  Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: molecular genetic evidence for deletions.

Authors:  U Francke; J F Harper; B T Darras; J M Cowan; E R McCabe; A Kohlschütter; W K Seltzer; F Saito; J Goto; J P Harpey
Journal:  Am J Hum Genet       Date:  1987-03       Impact factor: 11.025

10.  X-linked congenital adrenal hypoplasia. A study of five generations of a Greenlandic Family.

Authors:  K E Petersen; T Bille; B B Jacobsen; T Iversen
Journal:  Acta Paediatr Scand       Date:  1982-11
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  2 in total

1.  A new nonsyndromic X-linked sensorineural hearing impairment linked to Xp21.2.

Authors:  A K Lalwani; J R Brister; J Fex; K M Grundfast; A T Pikus; B Ploplis; T San Agustin; H Skarka; E R Wilcox
Journal:  Am J Hum Genet       Date:  1994-10       Impact factor: 11.025

2.  X-linked progressive mixed deafness: a new microdeletion that involves a more proximal region in Xq21.

Authors:  C Piussan; A Hanauer; N Dahl; M Mathieu; C Kolski; V Biancalana; S Heyberger; V Strunski
Journal:  Am J Hum Genet       Date:  1995-01       Impact factor: 11.025

  2 in total

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