Last edited by Mikaramar
Sunday, July 26, 2020 | History

7 edition of The Official Parent"s Sourcebook on Niemann-Pick Disease found in the catalog.

The Official Parent"s Sourcebook on Niemann-Pick Disease

A Revised and Updated Directory for the Internet Age

by ICON Health Publications

  • 5 Want to read
  • 36 Currently reading

Published by Icon Health Publications .
Written in English


The Physical Object
Number of Pages312
ID Numbers
Open LibraryOL7581571M
ISBN 100597830258
ISBN 109780597830259
OCLC/WorldCa53922273

  The title of this book includes the word official. This reflects the fact that the sourcebook draws from public, academic, government, and peer-reviewed research.   Niemann-Pick disease is an inherited condition involving lipid metabolism, which is the breakdown, transport, and use of fats and cholesterol in the body. In people with this condition, abnormal lipid metabolism causes harmful amounts of lipids to accumulate in .

Books on Genetic Diseases - Health, Diseases and Disorders The Official Patient's Sourcebook on Machado-Joseph Disease: A Revised and Updated Directory for the Internet Age by Icon Health Publications The Official Parent's Sourcebook on Friedreich's Ataxia: A Revised and Updated Directory for the Internet Age. Niemann-Pick disease (NPD) is a group of diseases passed down through families (inherited) in which fatty substances called lipids collect in the cells of the spleen, liver, and brain. There are three common forms of the disease.

Niemann-Pick disease type C (NP-C) is a rare autosomal-recessively inherited lysosomal storage disorder. It is caused by mutations in the NPC1 (95%) or NPC2 gene. It is a progressive and highly heterogeneous disease, characterized by the presentation of . Niemann-Pick disease is a condition that affects many body systems. It has a wide range of symptoms that vary in severity. Niemann-Pick disease is divided into four main types: type A, type B, type C1, and type C2. These types are classified on the basis of genetic cause and the signs and symptoms of the s with Niemann-Pick disease type A usually develop an enlarged liver and.


Share this book
You might also like
place-names of Devon

place-names of Devon

Why Britain needs a social market economy

Why Britain needs a social market economy

Profile of Brong Kyempim

Profile of Brong Kyempim

Dictionary of optics and precision engineering.

Dictionary of optics and precision engineering.

Idea into art

Idea into art

Close to home.

Close to home.

Managing the environment, managing ourselves

Managing the environment, managing ourselves

Heath Middle Level Literature

Heath Middle Level Literature

Review and assessment of research relevant to design aspects of nuclear power plant piping systems

Review and assessment of research relevant to design aspects of nuclear power plant piping systems

Law of Evidence

Law of Evidence

Small Business Lending Enhancing Act of 1995

Small Business Lending Enhancing Act of 1995

The Official Parent"s Sourcebook on Niemann-Pick Disease by ICON Health Publications Download PDF EPUB FB2

The Official Parent's Sourcebook on Niemann-Pick Disease: A Revised and Updated Directory for the Internet Age [Icon Health Publications] on *FREE* shipping on qualifying offers. The Official Parent's Sourcebook on Niemann-Pick Disease: A Revised and Updated Directory for the Internet Age.

The Official Parent's Sourcebook on Refsum Disease: A Revised and Updated Directory for the Internet Age [Icon Health Publications] on *FREE* shipping on qualifying offers. This sourcebook has been created for parents who have decided to make education and Internet-based research an integral part of the treatment process.

Although it gives information useful First published: 12 Sep,   The Official Parent's Sourcebook on Batten Disease: A Revised and Updated Directory for the Internet Age by Icon Health Publications (Author) ISBN ISBN Why is ISBN important.

ISBN. This bar-code number lets you verify that you're getting exactly the right version or edition of a book. The digit and   The Official Parent's Sourcebook on Menkes Disease: A Revised and Updated Directory for the Internet Age [Icon Health Publications] on *FREE* shipping on qualifying offers.

The Official Parent's Sourcebook on Menkes Disease: A Author: Icon Health Publications. The title of this book includes the word official. This reflects the fact that the sourcebook draws from public, academic, government, and peer-reviewed research.

Selected readings from various agencies are reproduced to give you some of the latest official information available to date on gaucher's published: 09 Sep, Get this from a library. The official parent's sourcebook on Menkes disease. [James N Parker; Philip M Parker;] -- This book has been created for parents who have decided to make education and research an integral part of the treatment process.

Although it also. All types of Niemann-Pick are autosomal recessive. This means that both parents are carriers. Each parent has 1 copy of the abnormal gene without having any signs of the disease themselves.

When both parents are carriers, there is a 25% chance that their child will have the disease and a 50% chance that their child will be a carrier.

Niemann–Pick disease is a group of severe inherited metabolic disorders, in which sphingomyelin accumulates in lysosomes in cells (the lysosomes normally transport material through and out of cells). These disorders involve the dysfunctional metabolism of sphingolipids, which are fats found in cell membranes (so it is a kind of sphingolipidosis, which is included in the larger family of.

The title of this book includes the word official. This reflects the fact that the sourcebook draws from public, academic, government, and peer-reviewed research. Selected readings from various agencies are reproduced to give you some of the latest official information available to date on addison's disease.

Title: The Official Parents Sourcebook On Menkes Dis, Author: Larita Cory, Name: The Official Parents Sourcebook On Menkes Dis, Length: 5 pages, Page: 1, Published: Issuu company logo Issuu. 1. Introduction.

Niemann-Pick disease (NPD) type A (NPD-A, OMIM ) or type B (NPD-B, OMIM ) are caused by mutations in the sphingomyelin phosphodiesterase-1 gene (SMPD1, OMIM ; NG_ reference sequence) on 11p that encodes for the acid sphingomyelinase enzyme (ASM, E.C.#, SMPD1).ASM catalyzes the hydrolytic cleavage.

Get this from a library. The official parent's sourcebook on Tay-Sachs disease. [James N Parker; Philip M Parker; Icon Group International, Inc.;] -- This book has been created for parents who have decided to make education and research an integral part of the treatment process.

Although it also gives information useful to doctors, caregivers and. The Official Parent's Sourcebook on Menkes Disease by ICON Health Publications, SeptemberIcon Health Publications edition, in English. The Niemann-Pick gene mutations are passed from parents to children in a pattern called autosomal recessive inheritance.

This means that both the mother and the father must pass on the defective form of the gene for the child to be affected. Niemann-Pick is a progressive disease, and there is no cure.

It can occur at any age. Types of Niemann-Pick. Get this from a library. The Official Parent's Sourcebook on Childhood Hodgkin's Disease.

[James N Parker; Philip M Parker] -- This book has been created for parents who have decided to make education and research an integral part of the treatment process. Although it also gives information useful to doctors, caregivers and. The Official Patient's Sourcebook on Addison's Disease book.

Read 2 reviews from the world's largest community for readers. This sourcebook has been crea 4/5(2). Electronic books Bibliography Popular works: Additional Physical Format: Print version: Official parent's sourcebook on childhood Hodgkin's disease.

San Diego, Calif.: Icon Health Publications, © Material Type: Document, Internet resource: Document Type: Internet Resource, Computer File: All Authors / Contributors. Introduction. Niemann-Pick (NP) disease is caused by an abnormality in lysosomes, which are unable to degrade macromolecules; as a result, the latter accumulate inside these organelles to form cellular inclusions ().NP disease encompasses a set of autosomal recessive hereditary abnormalities characterized by the accumulation of lipids, mostly sphingomyelin and cholesterol, in.

Niemann-Pick Disease is always fatal. In Type C, the sufferers usually die before the age of 20 years. Moreover, some of them die before 10 years. Acid sphingomyelinase enzyme deficiency results in Niemann-Pick Disease, type A and B. Individuals suffering from the type A Niemann-Pick Disease (NPA) usually die between the ages of 2 to 4 years.

COVID Resources. Reliable information about the coronavirus (COVID) is available from the World Health Organization (current situation, international travel).Numerous and frequently-updated resource results are available from this ’s WebJunction has pulled together information and resources to assist library staff as they consider how to handle coronavirus.

The National Niemann-Pick Disease Foundation (NNPDF) does not engage in the practice of medicine. It is not a medical authority nor does it claim to have medical knowledge. This site is an educational service of the National Niemann-Pick Disease Foundation and is not meant to provide diagnostic or treatment advice.ICON Health Publications has 74 books on Goodreads with ratings.

ICON Health Publications’s most popular book is The Official Patient's Sourcebook on.The Official Parent's Sourcebook On Joubert Syndrome: A Revised And Updated Directory For The Internet Age - Icon Health Publications. DOWNLOAD HERE.