Infantile Hypophosphatasia: Clinical Case

Infantile Hypophosphatasia: Clinical Case

Background. Hypophosphatasia is rare hereditary disease caused by deficiency of the tissue-nonspecific alkaline phosphatase isozyme. It manifests with bone and teeth mineralisation defects, electrolyte imbalance, respiratory disorders, convulsive syndrome, physical developmental delay, nephrocalcino...

Deskribapen osoa

Xehetasun bibliografikoak
Egile Nagusiak:	Tatyana V. Gabrusskaya, Yana V. Panutina, Maria O. Revnova, Mikhail M. Kostik
Formatua:	Artikulua
Hizkuntza:	English
Argitaratua:	"Paediatrician" Publishers LLC 2020-02-01
Saila:	Вопросы современной педиатрии
Gaiak:	children hypophosphatasia rickets-like diseases alkaline phosphatase asfotase alfa alpl gene
Sarrera elektronikoa:	https://vsp.spr-journal.ru/jour/article/view/2259

Antzeko izenburuak

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