Proprotein convertase 1/3 (PC1/3) deficiency is a very rare disease characterized by severe intractable diarrhea in the first years of life, followed by obesity and several hormonal deficiencies later. Diabetes mellitus requiring insulin treatment and diabetic ketoacidosis have not been reported in this disorder. We herein present a girl with PC1/3 deficiency who has been followed from birth to 17 years of age. She developed deficiencies of all pituitary hormones over time as well as diabetes mellitus while receiving growth hormone (GH) therapy. She was complicated with diabetic ketoacidosis during dietary management of diabetes mellitus, thus insulin treatment was initiated. Insulin requirement to regulate hyperglycemia was short-lived. Re...
Context: Biallelic mutations in NEUROG3 are known to cause early-onset malabsorptive diarrhea due to...
This is the author accepted manuscript. The final version is available from the publisher via the DO...
An increased frequency of diabetes or impaired glucose tolerance in Klinefelter���s syndrome has bee...
BACKGROUND & AIMS Proprotein convertase 1/3 (PC1/3) deficiency, an autosomal-recessive disorder c...
Background: Growth failure and growth hormone deficiency (GHD) have been reported as one accessory f...
GoalsThe aim of this report is to delineate the clinical, pathologic, and enteroendocrine (EE) featu...
Introduction: Mauriac syndrome is a severe form of growth retardation seen in patients with poorly c...
GOALS The aim of this report is to delineate the clinical, pathologic, and enteroendocrine (EE) f...
Diabetes mellitus develops in about 10% of acromegalic patients, usually secondary to insulin resist...
In a seminal report, a 17-year-old boy with panhypopituitarism had fatty liver (FL) amelioration wit...
Issue: To report a homozygous pathogenic variant in PCSK1 in a boy affected with proprotein converta...
Item does not contain fulltextBACKGROUND: Typical cases of glucose transporter-1 deficiency syndrome...
Type 1 diabetes mellitus (T1DM) is the most common diabetes type among children, causing more than ...
Kearns – Sayre syndrome (KSS) is a rare mitochondriopathy. Among chronic progressive external ophtha...
Glucose transporter type 1 deficiency syndrome (Glut-1DS) is caused by autosomal dominant haplodefic...
Context: Biallelic mutations in NEUROG3 are known to cause early-onset malabsorptive diarrhea due to...
This is the author accepted manuscript. The final version is available from the publisher via the DO...
An increased frequency of diabetes or impaired glucose tolerance in Klinefelter���s syndrome has bee...
BACKGROUND & AIMS Proprotein convertase 1/3 (PC1/3) deficiency, an autosomal-recessive disorder c...
Background: Growth failure and growth hormone deficiency (GHD) have been reported as one accessory f...
GoalsThe aim of this report is to delineate the clinical, pathologic, and enteroendocrine (EE) featu...
Introduction: Mauriac syndrome is a severe form of growth retardation seen in patients with poorly c...
GOALS The aim of this report is to delineate the clinical, pathologic, and enteroendocrine (EE) f...
Diabetes mellitus develops in about 10% of acromegalic patients, usually secondary to insulin resist...
In a seminal report, a 17-year-old boy with panhypopituitarism had fatty liver (FL) amelioration wit...
Issue: To report a homozygous pathogenic variant in PCSK1 in a boy affected with proprotein converta...
Item does not contain fulltextBACKGROUND: Typical cases of glucose transporter-1 deficiency syndrome...
Type 1 diabetes mellitus (T1DM) is the most common diabetes type among children, causing more than ...
Kearns – Sayre syndrome (KSS) is a rare mitochondriopathy. Among chronic progressive external ophtha...
Glucose transporter type 1 deficiency syndrome (Glut-1DS) is caused by autosomal dominant haplodefic...
Context: Biallelic mutations in NEUROG3 are known to cause early-onset malabsorptive diarrhea due to...
This is the author accepted manuscript. The final version is available from the publisher via the DO...
An increased frequency of diabetes or impaired glucose tolerance in Klinefelter���s syndrome has bee...