Cargando…
Hypophosphatasia Presenting with Pyridoxine-Responsive Seizures, Hypercalcemia, and Pseudotumor Cerebri: Case Report
Hypophosphatasia (HPP) is an inborn error of metabolism characterized by defective bone mineralization caused by a deficiency in alkaline phosphatase (ALP) activity due to mutations in the tissue-nonspecific ALP (TNALP) gene. The clinical expression of the disease is variable. Six forms of HPP are i...
Autores principales: | Demirbilek, Hüseyin, Alanay, Yasemin, Alikaşifoğlu, Ayfer, Topçu, Meral, Mornet, Etienne, Özön, Alev, Kandemir, Nurgün |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Galenos Publishing
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3316461/ https://www.ncbi.nlm.nih.gov/pubmed/22394703 http://dx.doi.org/10.4274/jcrpe.473 |
Ejemplares similares
-
GnRH Stimulation Test in Precocious Puberty: Single Sample is Adequate for Diagnosis and Dose Adjustment
por: Kandemir, Nurgün, et al.
Publicado: (2011) -
Long-Term Follow-up of a Case with Proprotein Convertase 1/3 Deficiency: Transient Diabetes Mellitus with Intervening Diabetic Ketoacidosis During Growth Hormone Therapy
por: Gönç, E. Nazlı, et al.
Publicado: (2017) -
The Relationship Between Serum Adiponectin, Tumor Necrosis Factor−Alpha, Leptin Levels and Insulin Sensitivity in Childhood and Adolescent Obesity: Adiponectin is a Marker of Metabolic Syndrome
por: Alikaşifoğlu, Ayfer, et al.
Publicado: (2009) -
Severe Undervirilisation in a 46,XY Case Due to a Novel Mutation in HSD17B3 Gene
por: Alikaşifoğlu, Ayfer, et al.
Publicado: (2015) -
Growth Hormone Deficiency in a Child with Neurofibromatosis-Noonan Syndrome
por: Vurallı, Doğuş, et al.
Publicado: (2016)