Bangstad syndrome

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Bangstad syndrome
Other namesAtaxia-diabetes-goiter-gonadal insufficiency syndrome
Autosomal recessive - en.svg
This condition is inherited in an autosomal recessive manner

Bangstad syndrome is a severe, inherited congenital disorder associated with abnormalities of the cell membrane.

It was characterized in 1989 by H. J. Bangstad.[1]

Presentation

Presenting at birth,[2] features of the disorder include moderately severe IUGR, microcephaly, craniosynostosis, moderately severe post-uterine growth retardation, deafness, deep-set eyes, cryptorchidism, truncal obesity[clarification needed] and acanthosis nigricans, small teeth, prognathism, dislocated radial heads without generalized skeletal dysplasia, however, tall vertebrae, moderate mental retardation, hypothyroidism, insulin resistance, hypoparathyroidism.[3]

Diagnosis

Thyroid-stimulating hormone, parathyroid hormone, luteinizing hormone, follicle-stimulating hormone, adrenocorticotropic hormone, glucagon, and insulin levels in the blood are usually elevated.[3]

Treatment

References

  1. Bangstad HJ; Beck-Nielsen H; Hother-Nielsen O et al. (May 1989). "Primordial birdheaded nanism associated with progressive ataxia, early onset insulin resistant diabetes, goiter and primary gonadal insufficiency. A new syndrome". Acta Paediatr Scand 78 (3): 488–93. doi:10.1111/j.1651-2227.1989.tb11119.x. PMID 2662702. 
  2. Bruno Bissonnette; Igor Luginbuehl; Bernard J. Dalens (20 July 2006). Syndromes: rapid recognition and perioperative implications. McGraw-Hill Professional. pp. 92–. ISBN 978-0-07-135455-4. https://books.google.com/books?id=uRR1MYa-w5wC&pg=PT92. Retrieved 29 June 2010. 
  3. 3.0 3.1 "Bangstad syndrome". January 8, 2021. https://rarediseases.info.nih.gov/diseases/812/bangstad-syndrome. 

External links

Classification
External resources




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