Cystic Fibrosis Archives

Chronic Kidney Disease

Secondary Osteoporosis

What is Secondary Osteoporosis? Osteoporosis is a condition where the structure of the bones weakens, making …

Bowel Obstruction

Meconium Ileus

What is Meconium Ileus? In newborn babies, a condition called meconium ileus (MI) is one of …

Chronic Pancreatitis

Hyperglycemia

What is Hyperglycemia? “Hyperglycemia” is a term from Greek that translates to “high sugar blood”. This …

constipation

Pediatric Rectal Prolapse

What is Pediatric Rectal Prolapse? Rectal prolapse means some or all of the lining of your …

COPD

Pulmonary Hypertension Due to Lung Disease or Hypoxia

What is Pulmonary Hypertension Due to Lung Disease or Hypoxia? Pulmonary hypertension (PH) is a serious …

Further Cystic Fibrosis Topics

45,X with Mosaicism Albright Hereditary Osteodystrophy Alkaptonuria alpha-dystroglycanopathies Becker Dystrophy Beckwith-Wiedemann Syndrome Bethlehem Dystrophy Birt-Hogg-Dube syndrome BRCA1 and BRCA2 Cayler Cardio-Facial Syndrome Channelopathy Congenital Heart Disease Corneal Dystrophy Cornelia de Lange Syndrome Cri Du Chat Syndrome Crigler-Najjar Cystic Fibrosis De Barsy Syndrome DiGeorge Syndrome Down Syndrome Duchenne Muscular Dystrophy Ehlers Danlos Syndrome Enzyme Deficiencies Familial Adenomatous Polyposis Familial Aldosteronism Familial Combined Hyperlipidemia Familial Htpertriglyceridemia Familial Hypercholesterolemia Familial Hypoalphalipoproteinemia Familial Hypocalciuric Hypercalcemia Fragile X Syndrome Friedreich Ataxia Fuchs Endothelial Corneal Dystrophy Gardenr Syndrome Genetic Kidney Disease Gilbert Syndrome Gorlin-Goltz Syndrome Growth Failure Hereditary Angioedema Hereditary Ataxia Homocystinuria Human Leukocyte Antigen B27 Hypoxanthine-Guanine Phosphoribosyltransferase (HPRT) Enzyme Deficiency Inborn Errors of Metabolism Infantile Refsum Disease (IRD) Kartagener Syndrome Lesch-Nyhan Syndrome Liddle Syndrome Liver Disease Lucy-Driscoll Syndrome Lynch Syndrome Lysosomal Storage Disease Lysosomal Storage Diseases Marfan Syndrome Metabolic Myopathy Mitochondrial Disorders Monosomy X (45,XO) Multiple Endocrine Neoplasia 1 Muscular Dystrophy Myotonic Dystrophy Neonatal Adrenoleukodystrophy (NALD) Neurocognitive Deficits Ophthalmologic Abnormalities Plummer-Vinson Syndrome Pseudohypoparathyroidism Respiratory Diseases Rhizomelic Chondrodysplasia Punctata Type 1 (RCDP1) Sex Chromosome Trisomy Situs Inversus Totalis Skeletal Anomalies Spinocerebellar Ataxia Tuberous Sclerosis Turcot Syndrome Von Hippel-Lindau Syndrome X-Linked Disorders XYY Zellweger Syndrome

Child Health

Echogenic Bowel

Published: July 15, 2024

What is Echogenic Bowel? “Fetal echogenic bowel” refers to a condition noticed on a prenatal ultrasound …

15 Jul 24

Cystic Fibrosis

Cystic Fibrosis and Liver Disease

Published: July 15, 2024

What is Cystic Fibrosis and Liver Disease? Cystic fibrosis, or CF, is a genetic disorder that …

15 Jul 24

Cystic Fibrosis

Cystic Fibrosis–Related Diabetes

Published: July 15, 2024

What is Cystic Fibrosis–Related Diabetes? Cystic fibrosis-related diabetes (CFRD) is a complication of cystic fibrosis (CF), …

15 Jul 24

Cystic Fibrosis

Published: July 15, 2024

What is Cystic Fibrosis? Cystic fibrosis is a disease that has affected children worldwide since ancient …

15 Jul 24

Agitation & Violent Behavior

Vitamin D Deficiency

Published: July 9, 2024

What is Vitamin D Deficiency? Vitamin D, a type of vitamin that dissolves in fat, is …

9 Jul 24

Further Cystic Fibrosis Topics

45,X with Mosaicism

Albright Hereditary Osteodystrophy

Alkaptonuria

alpha-dystroglycanopathies

Becker Dystrophy

Beckwith-Wiedemann Syndrome

Bethlehem Dystrophy

Birt-Hogg-Dube syndrome

BRCA1 and BRCA2

Cayler Cardio-Facial Syndrome

Channelopathy

Congenital Heart Disease

Corneal Dystrophy

Cornelia de Lange Syndrome

Cri Du Chat Syndrome

Crigler-Najjar

Cystic Fibrosis

Articles

Further Cystic Fibrosis Topics

45,X with Mosaicism

Albright Hereditary Osteodystrophy

Alkaptonuria

alpha-dystroglycanopathies

Becker Dystrophy

Beckwith-Wiedemann Syndrome

Bethlehem Dystrophy

Birt-Hogg-Dube syndrome

BRCA1 and BRCA2

Cayler Cardio-Facial Syndrome

Channelopathy

Congenital Heart Disease

Corneal Dystrophy

Cornelia de Lange Syndrome

Cri Du Chat Syndrome

Crigler-Najjar

Cystic Fibrosis

De Barsy Syndrome

DiGeorge Syndrome

Down Syndrome

Duchenne Muscular Dystrophy

Ehlers Danlos Syndrome

Enzyme Deficiencies

Familial Adenomatous Polyposis

Familial Aldosteronism

Familial Combined Hyperlipidemia

Familial Htpertriglyceridemia

Familial Hypercholesterolemia

Familial Hypoalphalipoproteinemia

Familial Hypocalciuric Hypercalcemia

Fragile X Syndrome

Friedreich Ataxia

Fuchs Endothelial Corneal Dystrophy

Gardenr Syndrome

Genetic Kidney Disease

Gilbert Syndrome

Gorlin-Goltz Syndrome

Growth Failure

Hereditary Angioedema

Hereditary Ataxia

Homocystinuria

Human Leukocyte Antigen B27

Hypoxanthine-Guanine Phosphoribosyltransferase (HPRT) Enzyme Deficiency

Inborn Errors of Metabolism

Infantile Refsum Disease (IRD)

Kartagener Syndrome

Lesch-Nyhan Syndrome

Liddle Syndrome

Liver Disease

Lucy-Driscoll Syndrome

Lynch Syndrome

Lysosomal Storage Disease

Lysosomal Storage Diseases

Marfan Syndrome

Metabolic Myopathy

Mitochondrial Disorders

Monosomy X (45,XO)

Multiple Endocrine Neoplasia 1

Muscular Dystrophy

Myotonic Dystrophy

Neonatal Adrenoleukodystrophy (NALD)

Neurocognitive Deficits

Ophthalmologic Abnormalities

Plummer-Vinson Syndrome

Pseudohypoparathyroidism

Respiratory Diseases

Rhizomelic Chondrodysplasia Punctata Type 1 (RCDP1)

Sex Chromosome Trisomy

Situs Inversus Totalis

Skeletal Anomalies

Spinocerebellar Ataxia

Tuberous Sclerosis

Turcot Syndrome

Von Hippel-Lindau Syndrome

X-Linked Disorders

XYY

Zellweger Syndrome

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