Arthritis, and Hypoglycemia

Diseases related with Arthritis and Hypoglycemia

In the following list you will find some of the most common rare diseases related to Arthritis and Hypoglycemia that can help you solving undiagnosed cases.


Top matches:

Low match LARON SYNDROME


Laron syndrome is a congenital disorder characterized by marked short stature associated with normal or high serum growth hormone (GH) and low serum insulin-like growth factor-1 (IGF-I) levels which fail to rise after exogenous GH administration.

LARON SYNDROME Is also known as complete growth hormone insensitivity|primary growth hormone insensitivity|gh receptor deficiency|growth hormone receptor deficiency|laron-type dwarfism|short stature due to growth hormone resistance|pituitary dwarfism ii|primary growth hormone resistance

Related symptoms:

  • Intellectual disability
  • Micrognathia
  • Abnormal facial shape
  • Motor delay
  • Brachydactyly


SOURCES: ORPHANET MENDELIAN

More info about LARON SYNDROME

Low match GLYCOGEN STORAGE DISEASE IC; GSD1C


GLYCOGEN STORAGE DISEASE IC; GSD1C Is also known as gsd ic

Related symptoms:

  • Hypertension
  • Hepatomegaly
  • Renal insufficiency
  • Hypoglycemia
  • Proteinuria


SOURCES: ORPHANET OMIM MENDELIAN

More info about GLYCOGEN STORAGE DISEASE IC; GSD1C

Low match GLYCOGEN STORAGE DISEASE DUE TO GLUCOSE-6-PHOSPHATASE DEFICIENCY TYPE IB


Glycogenosis due to glucose-6-phosphatase deficiency (G6P) type b, or glycogen storage disease (GSD) type 1b, is a type of glycogenosis due to G6P deficiency (see this term).

GLYCOGEN STORAGE DISEASE DUE TO GLUCOSE-6-PHOSPHATASE DEFICIENCY TYPE IB Is also known as glycogenosis due to glucose-6-phosphatase transport defect type ib|gsd type ib|glycogenosis due to glucose-6-phosphatase deficiency type 1b|glycogen storage disease type ib|gsd due to g6p deficiency type ib|glycogen storage disease due to g6p deficiency t

Related symptoms:

  • Seizures
  • Short stature
  • Growth delay
  • Hypertension
  • Hepatomegaly


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about GLYCOGEN STORAGE DISEASE DUE TO GLUCOSE-6-PHOSPHATASE DEFICIENCY TYPE IB

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Other less relevant matches:

Low match GROWTH HORMONE INSENSITIVITY WITH IMMUNODEFICIENCY


GROWTH HORMONE INSENSITIVITY WITH IMMUNODEFICIENCY Is also known as growth hormone insensitivity due to postreceptor defect|laron syndrome due to postreceptor defect

Related symptoms:

  • Intellectual disability
  • Seizures
  • Short stature
  • Hearing impairment
  • Growth delay


SOURCES: OMIM MENDELIAN

More info about GROWTH HORMONE INSENSITIVITY WITH IMMUNODEFICIENCY

Low match GLYCOGEN STORAGE DISEASE IA; GSD1A


Glycogen storage disease type I, also known as von Gierke disease, typically manifests during the first year of life with severe hypoglycemia and hepatomegaly caused by the accumulation of glycogen. Affected individuals exhibit growth retardation, delayed puberty, lactic acidemia, hyperlipidemia, hyperuricemia, and in adults a high incidence of hepatic adenomas (summary by Lei et al., 1993).

GLYCOGEN STORAGE DISEASE IA; GSD1A Is also known as gsd1|hepatorenal form of glycogen storage disease|hepatorenal glycogenosis|glucose-6-phosphatase deficiency|gsd ia|von gierke disease|glycogen storage disease i

Related symptoms:

  • Seizures
  • Short stature
  • Growth delay
  • Neoplasm
  • Muscular hypotonia


SOURCES: ORPHANET OMIM MENDELIAN

More info about GLYCOGEN STORAGE DISEASE IA; GSD1A

Low match IMMUNE DYSREGULATION-POLYENDOCRINOPATHY-ENTEROPATHY-X-LINKED SYNDROME


Immunodysregulation - polyendocrinopathy - enteropathy - X-linked (IPEX) syndrome is a severe congenital systemic autoimmune disease characterized by refractory diarrhea, endocrinopathies, cutaneous involvement, and infections.

IMMUNE DYSREGULATION-POLYENDOCRINOPATHY-ENTEROPATHY-X-LINKED SYNDROME Is also known as enteropathy, autoimmune, with hemolytic anemia and polyendocrinopathy|ipex|autoimmune enteropathy type 1|iddm-secretory diarrhea syndrome|x-linked autoimmunity-allergic dysregulation syndrome|polyendocrinopathy, immune dysfunction, and diarrhea, x-linked|

Related symptoms:

  • Growth delay
  • Failure to thrive
  • Anemia
  • Intrauterine growth retardation
  • Diarrhea


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about IMMUNE DYSREGULATION-POLYENDOCRINOPATHY-ENTEROPATHY-X-LINKED SYNDROME

Low match GLYCOGEN STORAGE DISEASE DUE TO LIVER GLYCOGEN PHOSPHORYLASE DEFICIENCY


Liver phosphorylase deficiency, or glycogen storage disease type 6b (Hers' disease, GSD 6b) is a benign and rare form of glycogen storage disease.

GLYCOGEN STORAGE DISEASE DUE TO LIVER GLYCOGEN PHOSPHORYLASE DEFICIENCY Is also known as liver glycogen phosphorylase deficiency|glycogen storage disease type vi|gsd type 6|glycogen storage disease type 6|gsd type vi|hepatic glycogen phosphorylase deficiency|glycogenosis type 6|gsd due to liver glycogen phosphorylase deficiency|glycogenosis t

Related symptoms:

  • Short stature
  • Hypoglycemia


SOURCES: ORPHANET MENDELIAN

More info about GLYCOGEN STORAGE DISEASE DUE TO LIVER GLYCOGEN PHOSPHORYLASE DEFICIENCY

Low match PYOGENIC STERILE ARTHRITIS, PYODERMA GANGRENOSUM, AND ACNE


PYOGENIC STERILE ARTHRITIS, PYODERMA GANGRENOSUM, AND ACNE Is also known as papas|familial recurrent arthritis|papa syndrome|fra

Related symptoms:

  • Diabetes mellitus
  • Arthritis
  • Proteinuria
  • Type I diabetes mellitus
  • Acne


SOURCES: OMIM MENDELIAN

More info about PYOGENIC STERILE ARTHRITIS, PYODERMA GANGRENOSUM, AND ACNE

Low match CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT 2; ADCAD2


Related symptoms:

  • Hypertension
  • Osteoporosis
  • Diabetes mellitus
  • Stroke
  • Sudden cardiac death


SOURCES: OMIM MESH MENDELIAN

More info about CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT 2; ADCAD2

Low match HEREDITARY ARTERIAL AND ARTICULAR MULTIPLE CALCIFICATION SYNDROME


Hereditary arterial and articular multiple calcification syndrome is a very rare genetic vascular disease of autosomal recessive inheritance, described in less than 20 patients to date, characterized by adult-onset (as early as the second decade of life) isolated calcification of the arteries of the lower extremities (including the iliac, femoral, and tibial arteries) as well as the capsule joints of the fingers, wrists, ankles and feet, and that usually manifests with mild paresthesias of the lower extremities, intense joint pain and swelling, and early onset arthritis of affected joints.

HEREDITARY ARTERIAL AND ARTICULAR MULTIPLE CALCIFICATION SYNDROME Is also known as calcification of joints and arteries|calja|acdc|arterial calcification due to deficiency of cd73

Related symptoms:

  • Pain
  • Diabetes mellitus
  • Arthralgia
  • Arthritis
  • Paresthesia


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about HEREDITARY ARTERIAL AND ARTICULAR MULTIPLE CALCIFICATION SYNDROME

Top 5 symptoms//phenotypes associated to Arthritis and Hypoglycemia

Symptoms // Phenotype % cases
Delayed puberty Uncommon - Between 30% and 50% cases
Short stature Uncommon - Between 30% and 50% cases
Hypertension Uncommon - Between 30% and 50% cases
Proteinuria Uncommon - Between 30% and 50% cases
Recurrent infections Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

Patients with Arthritis and Hypoglycemia. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases


Growth delay Hyperlipidemia Gout Diabetes mellitus Seizures Hepatomegaly Decreased glomerular filtration rate Hypercholesterolemia Lactic acidosis Osteoporosis Diarrhea Xanthelasma Xanthomatosis Focal segmental glomerulosclerosis Hepatocellular carcinoma

Rare Symptoms - Less than 30% cases


Acidosis Abnormal bleeding Elevated hepatic transaminase Intellectual disability Nephrolithiasis Type II diabetes mellitus Type I diabetes mellitus Atherosclerosis Hypertriglyceridemia Hepatitis Anemia Micrognathia Immune dysregulation Eczema Pancreatitis Intrauterine growth retardation Cognitive impairment Failure to thrive Neoplasm Doll-like facies Protuberant abdomen Hyperuricemia Lipemia retinalis Enlarged kidney High forehead Prematurely aged appearance Delayed eruption of teeth Microdontia Hypoplasia of penis Severe short stature Delayed skeletal maturation Brachydactyly Blue sclerae Depressed nasal ridge Motor delay Osteoarthritis Short toe Reduced number of teeth High pitched voice Truncal obesity Hypohidrosis Hypoplastic nasal bridge Aplasia/Hypoplasia involving the nose Underdeveloped supraorbital ridges Abnormality of the elbow Chronic pancreatitis Hepatoblastoma Renal insufficiency Hematuria Abnormal facial shape Metabolic acidosis Malnutrition Abnormality of the thyroid gland Hemolytic anemia Abnormality of the coagulation cascade Immunodeficiency Thyroiditis Ketoacidosis Autoimmune hemolytic anemia Erythroderma Hyperglycemia Thrombocytopenia Sepsis Nephritis Eosinophilia Abnormal intestine morphology Cardiac arrest Inflammatory abnormality of the skin Villous atrophy Hypothyroidism Autoimmunity Lymphadenopathy Nephrotic syndrome Generalized arterial calcification Sterile arthritis Ileus Rheumatoid arthritis Coronary artery calcification Arterial calcification Periarticular calcification Ectopic ossification Abnormal vascular morphology Intermittent claudication Hepatocellular adenoma Abnormality of cardiovascular system physiology Arterial tortuosity Gangrene Abnormal joint morphology Abnormality of the vertebral column Paresthesia Pancreatic hypoplasia Arthralgia Pain Glucose intolerance Myocardial infarction Sudden cardiac death Stroke Arterial occlusion Pyoderma gangrenosum Pyoderma Juvenile rheumatoid arthritis Acne Secretory diarrhea Intractable diarrhea Hypocitraturia Muscular hypotonia Distal renal tubular acidosis Prominent forehead Proportionate short stature External genital hypoplasia Keratitis Short long bone Increased body weight Lymphopenia Chronic diarrhea Abnormal lung morphology Progressive visual loss Growth hormone deficiency Deeply set eye Pneumonia Delayed menarche Obesity Respiratory distress Hearing impairment Oral ulcer Inflammation of the large intestine Recurrent bacterial infections Neutropenia Ketonemia Spider hemangioma Pulmonary arterial hypertension Abnormality of the endocrine system Abnormality of the skull Concave nasal ridge Lymphoid interstitial pneumonia Chronic hepatitis Portal hypertension Intermittent diarrhea Microalbuminuria Hypoglycemic seizures Pyelonephritis Enterocolitis Skeletal myopathy Fasting hypoglycemia Breathing dysregulation Neoplasm of the liver Renal tubular acidosis Prolonged bleeding time Decreased muscle mass Glomerulosclerosis Myopathy Elevated alkaline phosphatase Hypercalciuria Chronic kidney disease Venous thrombosis Nephrocalcinosis Epistaxis Full cheeks Nephropathy Hepatic failure Carcinoma Osteopenia Recurrent respiratory infections Decreased serum creatinine



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