Disease Comparison Results (show differences mode) for Familial progressive polyneuropathy and Laurence-Moon-Biedel syndrome

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Laurence-Moon-Biedel syndrome

Found: 76 | Differences: 67

Familial progressive polyneuropathy

Found: 29 | Differences: 20

Familial progressive polyneuropathy and Laurence-Moon-Biedel syndrome sharing 9 common findings. (show all, show common, show differences)

Clinical Manifestations
Signs & Symptoms
Delayed male adolescence/pubescence
Genital Hypoplasia/Male
Penis, small (Micropenis)
Scrotum small
Undescended testicles
Mental Deficiency Child
Weight gain
Bilateral Vision Loss
Narrow Palpebral Fissures
Visual Problems
Clinical Presentation & Variations
Presentation/Obese Retarded Blind Hypogenital male Youth
Presentation/Congenital Syndromes Renal failure
Presentation/Juvenile Cataract
Demographics & Risk Factors
Family History
Family history/Parental consanguinity
Sex & Age Groups
Population/Child-Infant Only
Population/Male
Laboratory Tests
Abnormal Lab Findings - Decreased
FSH/Follicle Stmulating Hormone/ICSH (Lab)
LH/Leutinizing Hormone (Lab)
Testosterone Total (Lab)
Diagnostic Test Results
Other Tests & Procedures
TEST/Failure of clomiphen to raise FSH/LH
Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs
Prader-Willi syndrome
Associated Disease & Complications - Causes
Blindness
Blindness, central
Cataract
Congenital heart disease
Congenital urinary tract malformations
Hereditary Blindness
Hypogenitalism/male
Hypogonadism, male
Infertility/sterility male
Laurence-Moon syndrome
Limb deformities/anomalies
Mental retardation
Microphallus deformity
Microphthalmos
Obesity
Obesity in Children
Obesity, massive
Paraplegia, spastic
Paraplegia, spastic hereditary
Pigmentary retinal dystrophy
Polydactyly/Supernumery digits
Renal anomalies
Renal Failure Chronic
Retinal Degeneration/Dystrophy
Retinitis pigmentosa
Retinopathy
Secondary male hypogonadism
Skull deformities
Strabismus, convergent
Tetralogy of Fallot
Genital Hypoplasia
Hand anomalies
Disease Mechanism & Classification
Class
CLASS/Pediatric disorders (ex)
CLASS/Systemic/no comment (category)
Pathophysiology
Pathophysiology/Gene locus Chromosome 16
Pathophysiology/Gene locus Chromosome 16q
Pathophysiology/Novel Gene BBS/LMB at 16q
Pathophysiology/Hypogonadotrophic hypogonadism
Pathophysiology/Secondary Testicular Failure
Pathophysiology/Hypothalamic pituitary dysfunction
Process
PROCESS/Autosomal recessive disorder (ex)
PROCESS/Hypogonadotropic hypogonadism/congenital
Synonyms
Synonym
Synonym/Bardet-Biedl syndrome
Clinical Manifestations
Signs & Symptoms
Symmetrical muscle/pain, weakness
Bilateral foot drop/signs
Neurological symptoms/signs
Paresthesias
Symmetric Polyneuropathy
Clinical Presentation & Variations
Presentation/Progressive Motor Sensory Polyneuropathy
Diagnostic Test Results
Pathology
BX/Nerve biopsy/abnormal
Electrodiagnosis
EMG/NCA Low amplitude
Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs
Diabetic peripheral neuropathy
Peroneal muscular atrophy/Charcot Marie Tooth
Associated Disease & Complications - Causes
Polyneuritis
Disease Mechanism & Classification
Class
CLASS/Neurologic (category)
CLASS/Peripheral nerve disease (ex)
Pathophysiology
Pathophysiology/Gene locus 12q24
Pathophysiology/Gene locus 12q24-qter
Pathophysiology/Gene locus chromosome 12
Pathophysiology/Hereditary disease/Adult manifestations
Pathophysiology/Hereditary Neuropathy
Treatment
Drug Therapy
SX/Nerve biopsy
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