A 6-Week-Old Boy with Neonatal Hypotonia and Feeding and Respiratory Difficulties

Author:

Ghosh Partha S.,Lidov Hart G. W.

Publisher

Springer International Publishing

Reference15 articles.

1. Bodensteiner JB. The evaluation of the hypotonic infant. Semin Pediatr Neurol. 2008;15:10–20.

2. Angulo MA, Butler MG, Cataletto ME. Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings. J Endocrinol Investig. 2015;38:1249–63.

3. Iannaccone ST, Castro D. Congenital muscular dystrophies and congenital myopathies. Continuum. 2013;19:1509–34.

4. Streib EW. AAEE minimonograph #27: differential diagnosis of myotonic syndromes. Muscle Nerve. 1987;10(7):603–15.

5. Brooke MH. Congenital fiber type disproportion. In: Kakulas BA, editor. Clinical studies in myology. Proceedings of the 2nd International Congress on Muscle Diseases, Perth, Australia, Nov. 22–29, 1971. Amsterdam: Exerpta Medica; 1973. p. 147–59.

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