Complex glycerol kinase deficiency usually presents with Duchenne muscular dystrophy, glycerol kinase deficiency and adrenal hypoplasia congenital. We describe a follow-up patient with complex glycerol kinase deficiency who had appropriate intrauterine development, but who at 1 month of age manifested severe growth delay and psychomotor retardation. Targeted therapy did not bring about the regression of symptoms: both bodyweight and height were below the 3rd centile until 8 years of age, and his Griffith's Mental Development scale score was 71 at age 5 years
Inherited metabolic diseases are a heterogeneous group of diseases caused by a punctual defect in ce...
Background . Congenital disorders of glycosylation (CDG) are a group of rare disorders in which glyc...
Four unrelated patients with glyceroluria ranging from 7 to 170 mmol/l were studied. The activity of...
Clinical follow-up of a case of complex glycerol kinase deficiency with severe body-growth and psych...
We demonstrate that isolated glycerol kinase (GK) deficiency in three families results from mutation...
Glycerol kinase deficiency (GKD, MIM 307030) is an X-linked recessive inborn error of metabolism occ...
A syndrome of Duchenne muscular dystrophy (DMD), adrenal hypoplasia, glycerol kinase deficiency, and...
X-linked adrenal hypoplasia congenita (AHC) is characterized by primary adrenal insufficiency caused...
Abstract Background Contiguous gene deletion syndromes are rare genomic disorders caused by deletion...
Contiguous gene deletions of chromosome Xp21 can lead to glycerol kinase deficiency and severe adren...
: The contiguous gene deletion syndromes (CGDS) are rare genomic disorders resulting from the deleti...
UNIV São Paulo,DEPT BIOL,MIOPATIAS LAB,São Paulo,BRAZILESCOLA PAULISTA MED SCH,BIOQUIM LAB,BR-04023 ...
Adenosine kinase (ADK) deficiency (OMIM [online mendelian inheritance in man]: 614300) is an autosom...
X-linked recessive disorder that presents in both iso-lated and complex forms. The contiguous deleti...
Congenital muscular dystrophies (CMD) are autosomal recessive infantile disorders characterized by d...
Inherited metabolic diseases are a heterogeneous group of diseases caused by a punctual defect in ce...
Background . Congenital disorders of glycosylation (CDG) are a group of rare disorders in which glyc...
Four unrelated patients with glyceroluria ranging from 7 to 170 mmol/l were studied. The activity of...
Clinical follow-up of a case of complex glycerol kinase deficiency with severe body-growth and psych...
We demonstrate that isolated glycerol kinase (GK) deficiency in three families results from mutation...
Glycerol kinase deficiency (GKD, MIM 307030) is an X-linked recessive inborn error of metabolism occ...
A syndrome of Duchenne muscular dystrophy (DMD), adrenal hypoplasia, glycerol kinase deficiency, and...
X-linked adrenal hypoplasia congenita (AHC) is characterized by primary adrenal insufficiency caused...
Abstract Background Contiguous gene deletion syndromes are rare genomic disorders caused by deletion...
Contiguous gene deletions of chromosome Xp21 can lead to glycerol kinase deficiency and severe adren...
: The contiguous gene deletion syndromes (CGDS) are rare genomic disorders resulting from the deleti...
UNIV São Paulo,DEPT BIOL,MIOPATIAS LAB,São Paulo,BRAZILESCOLA PAULISTA MED SCH,BIOQUIM LAB,BR-04023 ...
Adenosine kinase (ADK) deficiency (OMIM [online mendelian inheritance in man]: 614300) is an autosom...
X-linked recessive disorder that presents in both iso-lated and complex forms. The contiguous deleti...
Congenital muscular dystrophies (CMD) are autosomal recessive infantile disorders characterized by d...
Inherited metabolic diseases are a heterogeneous group of diseases caused by a punctual defect in ce...
Background . Congenital disorders of glycosylation (CDG) are a group of rare disorders in which glyc...
Four unrelated patients with glyceroluria ranging from 7 to 170 mmol/l were studied. The activity of...