Autosomal - GrepMed

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42 results

Autosomal Dominant Inheritance
- Most common mode of Mendelian inheritance
- Affected individual carries the

Autosomal Dominant ... one of a pair of autosomes ... #Autosomal #Dominant

Causes of Dilated Cardiomyopathy DCMP - Differential Diagnosis Algorithm
Idiopathic DCMP: Viral, Inflammatory cardiomyopathy, Genetic causes, Unknown

Genetically determined: Autosomal ... dominant, Autosomal

Marfan Syndrome - Signs and Symptoms

- Caused by mutations in the fibrillin-1 (FBN1) Gene (chromosome 15)
-

fibrillin function - Autosomal

Malignant Hyperpyrexia
A rare complciation of halothane or suxamethonium.
Predisposition to developing this is inherited (autosomal dominant).

#Malignant #Hyperpyrexia

is inherited (autosomal

$Inherited Non-hemolytic Disorders of Hyperbilirubinemia == Disorders of Conjugation == Gilbert Syndrome: • 5-10% of the population$

syndrome • An autosomal ... a super rare, autosomal ... Type II CN is an autosomal ... Syndrome: • Autosomal ... Dubin-Johnson: • Autosomal

Von Recklinghausen's Syndrome - Neurofibromatosis Type 1 (NF1)
Hereditary multiple neurofibromas.
Autosomal dominant with high rate

Autosomal dominant

Weight Gain / Obesity - Differential Diagnosis Algorithm
Decreased Expenditure:
• Sedentary Lifestyle
• Smoking Cessation

Genetic: • Autosomal ... Dominant • Autosomal

Peutz–Jeghers Syndrome
An autosomal dominant genetic disorder characterized by the development of benign hamartomatous polyps in the

Peutz–Jeghers Syndrome An autosomal

Cystic Fibrosis
An autosomal recessive condition. Mutations affect a specific gene on chromosome 7. The affected

Fibrosis An autosomal

Angioedema - Classification Diagnosis and Treatment
Types of Angioedema:
• Acute allergic angioedema - Usually occurs with

angioedema - Rare autosomal ... deficiency - Rare autosomal

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