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Disease Comparison Results (show all mode) for Beckwith-Wiedemann Syndrome and Hypogammaglobulinemia, cong. X-linked

Clinical
Demographics
Lab
Diagnostic
Diseases
Classification
Synonyms
Treatment
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Found: 42 | Differences: 32

Found: 217 | Differences: 207

Beckwith-Wiedemann Syndrome and Hypogammaglobulinemia, cong. X-linked sharing 10 common findings. (show all, show common, show differences)

Clinical Manifestations
Signs & Symptoms: Acute Diarrhea; Acute Diarrhea in Children; Chronic Diarrhea in a Child; Diarrhea; Diarrhea and Weight Loss; Diarrhea in Children; Diarrhea, chronic; Diarrhea, recurrent; Recurrent chest infections/bronchitis/sign
Disease Progression: Course/Chronic disorder; Course/Chronic only; Onset/Six months

Demographics & Risk Factors
Population Group: Child; Population/Pediatrics population
Family History: Family history/Immune defects
Sex & Age Groups: Population/Child; Population/Child-Infant Only; Population/Children/all

Laboratory Tests
Microbiology & Serology Findings: Common vaccination antibodies absent/low
Abnormal Lab Findings (Non Measured): Cytogenetics Abnormal; Absent/Low B-cells on Flow Cytometry; Flow cytometry tests/abnormal (Lab)
Abnormal Lab Findings - Decreased: Gamma globulin (Lab); IGG/Immunoglobulin G (Lab)

Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs: Cystic fibrosis (mucoviscidosis)
Associated Disease & Complications - Causes: Hypogammaglobulinemia; Hypogammaglobulinemia, acquired; Immunodeficiency; Infections; Lymphoblastic leukemia/acute

Disease Mechanism & Classification
Class: CLASS/Humoral Immune System Disorder (ex); CLASS/Pediatric disorders (ex); CLASS/Hematologic (category); CLASS/Spleen/thymus/RES/immune system (category)
Pathophysiology: Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations); Pathophysiology/Infection resistant to usual treatments; Pathophysiology/Proteins/blood disorder (ex); Pathophysiology/Poor immune resp/encapsulated bacteria; Pathophysiology/Poor slow recovery/ bacteria infection
Process: PROCESS/Hereditofamilial (category); PROCESS/Immunodeficiency disorder/Primary

Treatment
Drug Therapy: RX/Gamma globulin/prophylaxis/low dose

Clinical Manifestations
Signs & Symptoms: Hyperextensable Joints Infant; Macrosomia; Facial Asymmetry; Facial hemihypertrophy; Sunken Cheek Bones; Accessory nipples; Cardiomegaly/Heart dilatation; Port wine Stain Birthmark; Accelerated growth Child; Increased body length/newborn; Large baby/birth weight increased; Genitalia overgrowth/infant; Abdominal Mass; Abdominal Wall Defects; Everted umbilicus/prominent; Lax abdominal muscles; Hypoplasia Narrow Maxilla; Large tongue/macroglossia; Oral submucosal clefts; Tongue Protrudes Infant; Hepatosplenomegaly; Palpable Liver/Hepatomegaly; Delay Sitting Unsupported Infant; Hypotonia; Mouth Hangs Open Infant; Muscles Soft/Doughy Infant; Rolling Over Delay Infant; Babkin infant sign/Abnormal; Delayed walking milestone/child; Development Motor Skills (Milestones) Delayed; Galant Infant reflex/Abnormal; Head Neck Floppy Infant Hypotonia Sign; Infant Head Support Delay; Intelligence normal; Mental Deficiency Child; Moro reflex Poor/Absent Infant; Palmar Grasp infant Reflex Abnormal; Primitive infant reflexes/Abnormal; Progressive enlargement of Skull/infant; Rooting infant sign/Abnormal; Swimming infant reflex/Abnormal; Tonic Neck Infant reflex/Abnormal; Shallow Breathing Infant; Difficulty learning/school/workplace; Asymmetric Limbs; Cranial sutures ridging; Finger contractions/flexion (clinodactyly); Metopic sutures hypoplastic ridging; Sternum deformities; Tall child; Snoring; Splenomegaly; Dysmorphic appearance/face; Lateral Asymmetry; Tall Adult; Eyelid Retraction; Proptosis,bilateral; Asymmetric earlobes; Characteristic ear lobe crease; Ear lobe crease/Emperor Hadrian sign; Pits in Pinna/Congenital
Clinical Presentation & Variations: Presentation/Omphalocele Macroglossia Large neonate Hypoglycemia
Disease Progression: Course/Chronic disorder; Course/Chronic only; Course/Prognosis bad/usually; Course/Untreated mortality high

Demographics & Risk Factors
Population Group: Child; Infant; Population/Pediatrics population
Sex & Age Groups: Population/Child; Population/Child-Infant Only; Population/Children/all; Population/Infant; Population/Neonate-newborn

Laboratory Tests
Abnormal Lab Findings (Non Measured): Chromosomal abnormality (Lab); Fasting hypoglycemia (Lab)
Abnormal Lab Findings - Decreased: Glucose, blood (Lab)
Abnormal Lab Findings - Increased: Insulin C-Peptide type, serum (Lab); Insulin level (Lab); Proinsulin

Diagnostic Test Results
Pathology: PATH/Adrenocortical cytomegaly/hyperplasia; PATH/Testis Interstitial/Leydig hyperplasia; PATH/Pancreatic biopsy/Abnormal; PATH/Pancreatic islet cell hypertrophy/macrocytosis; PATH/Kidney dysplasia renal medulla; PATH/Visceromegaly
X-RAY: Xray/Large heart shadow/Chest; Xray/Soft tissue lateral neck/large tongue; Xray/Delayed fontanelle closure; Xray/Advanced bone age/child/adolescent; Xray/Advanced bone age/newborn
X-RAY With contrast: IVP/Bilateral large kidneys
Ultrasound: Ultrasound/Renal/Kidneys enlarged/symmetrical

Associated Diseases & Rule outs
Associated Disease & Complications: Acute respiratory failure/Respiratory arrest; Anal Atresia; Apnea, episodic; Atrial septal defect; Beckwith-Wiedemann syndrome; Cancer/malignancy; Carcinoid tumor of gut; Carcinoma, adrenal cortex; Carcinoma, hepatocellular; Childhood malignancy; Cleft Lip; Cleft lip/deformity; Cleft palate/deformity; CNS disease/involvement; Cognitive/learning disability; Colon atresia; Congenital diaphragmatic hernia; Congenital heart disease; Congenital urinary tract malformations; Cryptorchidism; Deafness, conduction type; Deafness, congenital; Encephalopathy, hypoglycemia; Encephalopathy/CNS effect; Exophthalmos; Gigantism; Glioblastoma/CNS; Gut Anomalies; Hemihypertrophy; Hepatoblastoma; Hip dislocation, congenital; Hydrocephalus; Hypercholesterolemia; Hypocalcemia; Hypoglycemia; Hypoglycemia, infantile; Hypoplasia left heart; Hypospadius anomaly; Ileal stenosis; Imperforate anus; Intestine malrotation; Liver Tumor; Lymphoma, non-Hodgkins type; Medullary sponge kidney disease; Meningoencephalocele; Meningomyelocele; Mental retardation; Microcephaly/oligophrenia; Multiple Congenital Anomalies; Multiple congenital anomalies/Mental retardation; Neonatal Hypotonia/Floppy Baby Syndrome; Neuroblastoma; Obesity; Obesity in Children; Obstructive sleep apnea/Children; Omphalocele; Organomegaly; Patent ductus arteriosis; Pectus carinatum/pigeon chest; Pectus excavatum; Plethora of newborn; Polycythemia rubra vera/infant; Polydactyly/Supernumery digits; Port wine nevus/Nevus flammeus/facial; Pulmonary artery branch/stenosis; Pyloric stenosis, cong. hypertrophic; Renal anomalies; Rhabdomyosarcoma; Rhabdomyosarcoma/muscle/extremity; Subdural hematoma; Teratoma; Tetralogy of Fallot; Umbilibal Anomalies; Umbilical hernia; Uterus Didelphus/Bicornuate; Ventricular septal defect; Wilms tumor/nephroblastoma; Hand anomalies

Disease Mechanism & Classification
Class: CLASS/Jablonski/NIH Archive Anomalies Database; CLASS/Pediatric disorders (ex); CLASS/Multisystem/organ involvement/pathology (ex); CLASS/Systemic/no comment (category)
Pathophysiology: Pathophysiology/Asymmetric deformities; Pathophysiology/Chromosome gene locus 11 (11p15) region; Pathophysiology/Dominant inheritance kindred/variety; Pathophysiology/Gene locus 11p15.5; Pathophysiology/Gene locus 5q35.3; Pathophysiology/Gene locus Chromosome 11; Pathophysiology/Gene locus Chromosome 5; Pathophysiology/Gene Locus Identified/OMIM database; Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations); Pathophysiology/Human p57(KIP2)at 11p15.5 involved; Pathophysiology/IGF2 (insulin-like growth factor II) gene involved; Pathophysiology/Intractable neonatal hypoglycemia; Pathophysiology/Pre-cancerous condition; Pathophysiology/Sporadic/hereditary/process; Pathophysiology/Leydig cell hypertrophy child; Pathophysiology/CTSA (Cathepsin A) Gene Mutation; Pathophysiology/Maternal Chromosome mutation
Process: PROCESS/Autosomal dominant hereditary disease (ex).; PROCESS/Congenital/developmental (category); PROCESS/Constitutional/essential disorder (ex); PROCESS/Eponymic (category); PROCESS/Genetic disorder/Spontaneous mutations/sporadic; PROCESS/Hereditary dominance/incomplete penetrance (ex).; PROCESS/Hereditofamilial (category); PROCESS/INCIDENCE/Esoteric disease (example); PROCESS/INCIDENCE/Rare disease (ex); PROCESS/Anomalies/Deformities/Malformations (EX)

Synonyms
Synonym: Synonym/Beckwith syndrome; Synonym/BWS (syndrome); Synonym/EMG Syndrome; Synonym/Exomphalos-macroglosia-gigantism/EMG; Synonym/Exomphalos-macroglossia-gigantism syndrome; Synonym/Hypoglycemia with macroglossia syndrome; Synonym/Macroglossia-omphalocele-visceromegaly syndrome; Synonym/Omphalocele-visceromegaly-macroglossia syndrome; Synonym/Visceromegaly-umbilical hernia-macroglossia syndrome; Synonym/Wiedemann II syndrome; Synonym/Wiedmann-Beckwith syndrome

Treatment
Drug Therapy: RX/Glucose
Other Treatments: TX/Constitutional/No definitive treatment

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