Detection of Inherited Neurometabolic Disorders: A Practical Clinical Approach  

Oleh:

Carballo, Enrique Chaves

Jenis: Article from Journal - ilmiah internasional
Dalam koleksi: Pediatric Clinics of North America vol. 39 no. 04 (Aug. 1992), page 801.

Ketersediaan

Perpustakaan FK Nomor Panggil: P13.K.1992.04 Non-tandon: 1 (dapat dipinjam: 0) Tandon: tidak ada

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Isi artikel

The most common neurometabolic disorders to be considered are organic acidurias and amino acid apathies followed by urea cycle disorders, congenital lactic acidosis, peroxisomal disorders, and, less frequently, sphingolipidoses, mucopolysaccharidoses, glycoprotein degradation disorders, fatty acid oxidation disorders, and neuronal ceroid lipofuscinoses.

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