eBook Atlas of Genetic Diagnosis and Counseling, 2nd Edition

  • Harold Chen
  • Published By:
  • ISBN-10: 1461410371
  • ISBN-13: 9781461410379
  • DDC: 616.042
  • Grade Level Range: College Freshman - College Senior
  • 2224 Pages | eBook
  • Original Copyright 2012 | Published/Released September 2013
  • This publication's content originally published in print form: 2012
  • Price:  Sign in for price

About

Overview

Dr. Chen shares his almost 40 years of clinical genetics practice in a comprehensive pictorial atlas of almost 250 genetic disorders, malformations, and malformation syndromes. The author provides a detailed outline for each disorder, describing its genetics, basic defects, clinical features, diagnostic tests, and counseling issues, including recurrence risk, prenatal diagnosis, and management. Numerous color photographs of prenatal ultrasounds, imagings, cytogenetics, and postmortem findings illustrate the clinical features of patients at different ages, patients with varying degrees of severity, and the optimal diagnostic strategies. The disorders cited are supplemented by case histories and diagnostic confirmation by cytogenetics, biochemical, and molecular techniques, when available. The Atlas of Genetic Diagnosis and Counseling will help all physicians to understand and recognize genetic diseases and malformation syndromes and better evaluate, counsel, and manage affected patients. In this new edition, 47 additional genetic disorders are added, as well as extensive updates made to the previous disorders. New illustrations, as previous edition, will be supplemented by case and family history, clinical features, and laboratory data, especially molecular confirmation.

Features and Benefits

  • Easy to use outline format.
  • Completely revised and expanded new edition.
  • Extensive up-to-date literature review for each disorder.

Table of Contents

Front Cover.
Half Title Page.
Title Page.
Other Frontmatter.
Copyright Page.
Dedication.
Preface to the Second Edition.
Preface to the First Edition.
Biography.
Table of Contents.
1: Acardia.
2: Achondrogenesis.
3: Achondroplasia.
4: Adams–Oliver Syndrome.
5: Agnathia.
6: Aicardi Syndrome.
7: Alagille Syndrome.
8: Albinism.
9: Alpha-Thalassemia X-linked Mental Retardation Syndrome.
10: Ambiguous Genitalia.
11: Amniotic Deformity, Adhesions, Mutilations (ADAM) Complex.
12: Androgen Insensitivity Syndrome.
13: Angelman Syndrome.
14: Apert Syndrome.
15: Aplasia Cutis Congenita.
16: Arthrogryposis Multiplex Congenita.
17: Asphyxiating Thoracic Dystrophy.
18: Ataxia-Telangiectasia.
19: Atelosteogenesis.
20: Autism.
21: Bannayan–Riley–Ruvalcaba Syndrome.
22: Beckwith–Wiedemann Syndrome.
23: Behcet Disease.
24: Biotinidase Deficiency.
25: Bladder Exstrophy.
26: Blepharophimosis, Ptosis, and Epicanthus Inversus Syndrome.
27: Body Stalk Anomaly.
28: Brachydactyly.
29: Branchial Cleft Anomalies.
30: Calcinosis Cutis.
31: Campomelic Dysplasia.
32: Carpenter Syndrome.
33: Cat Eye Syndrome.
34: Celiac Disease.
35: Cerebral Palsy.
36: Cerebro-Costo-Mandibular Syndrome.
37: Charcot–Marie–Tooth Disease.
38: CHARGE Syndrome.
39: Cherubism.
40: Chiari Malformation.
41: Chondrodysplasia Punctata.
42: Chromosome Abnormalities in Pediatric Solid Tumors.
43: Cleft Lip and/or Cleft Palate.
44: Cleidocranial Dysplasia.
45: Cloacal Exstrophy.
46: Clubfoot.
47: Collodion Baby.
48: Congenital Adrenal Hyperplasia.
49: Congenital Cutis Laxa.
50: Congenital Cytomegalovirus Infection.
51: Congenital Generalized Lipodystrophy.
52: Congenital Hemihyperplasia.
53: Congenital Hydrocephalus.
54: Congenital Hypothyroidism.
55: Congenital Muscular Dystrophy.
56: Congenital Toxoplasmosis.
57: Conjoined Twins.
58: Corpus Callosum Agenesis/Dysgenesis.
59: Craniometaphyseal Dysplasia.
60: Cri-Du-Chat Syndrome.
61: Crouzon Syndrome.
62: Cutis Marmorata Telangiectatica Congenita.
63: Cystic Fibrosis.
64: Dandy–Walker Malformation.
65: De Lange Syndrome.
66: Del(18p) Syndrome.
67: Del(22q11.2) Syndrome.
68: Del(Yq) Syndrome.
69: Diabetic Embryopathy.
70: Down Syndrome.
71: Duncan Syndrome.
72: Dyschondrosteosis.
73: Dysmelia.
74: Dysplasia Epiphysealis Hemimelica.
75: Dystonia.
76: Dystrophinopathies.
77: Ectrodactyly-Ectodermal Dysplasia-Clefting (EEC) Syndrome.
78: Ehlers-Danlos Syndrome.
79: Ellis-van Creveld Syndrome.
80: Enchondromatosis.
81: Epidermolysis Bullosa.
82: Epidermolytic Palmoplantar Keratoderma.
1: Faciogenital (Faciodigitogenital) Dysplasia.
2: Facioscapulohumeral Muscular Dystrophy.
3: Familial Adenomatous Polyposis.
4: Familial Hyperlysinemia.
5: Familial Mediterranean Fever.
6: Fanconi Anemia.
7: Femoral Hypoplasia – Unusual Facies Syndrome.
8: Fetal Akinesia Deformation Sequence.
9: Fetal Alcohol Spectrum Disorders.
10: Fetal Hydantoin Syndrome.
11: Fibrodysplasia Ossificans Progressiva.
12: Finlay–Marks Syndrome.
13: Floppy Infant.
14: Fragile X Syndrome.
15: Fraser Syndrome.
16: Freeman–Sheldon Syndrome.
17: Friedreich Ataxia.
18: Frontonasal Dysplasia.
19: Galactosemia.
20: Gastroschisis.
21: Gaucher Disease.
22: Generalized Arterial Calcification of Infancy.
23: Genitopatellar Syndrome.
24: Giant Congenital Melanocytic Nevi.
25: Glucose-6-Phosphate Dehydrogenase Deficiency.
26: Glycogen Storage Disease, Type II.
27: Goldenhar Syndrome.
28: Gorlin Syndrome.
29: Greig Cephalopolysyndactyly Syndrome.
30: Hallermann-Streiff Syndrome.
31: Harlequin Ichthyosis.
32: Hemophilia A.
33: Hereditary Hearing Loss.
34: Hereditary Hemochromatosis.
35: Hereditary Multiple Exostoses.
36: Herlyn-Werner-Wunderlich Syndrome.
37: Holoprosencephaly.
38: Holt-Oram Syndrome.
39: Huntington Disease.
40: Hydrolethalus Syndrome.
41: Hydrops Fetalis.
42: Hyper-IgE Syndrome.
43: Hypochondroplasia.
44: Hypoglossia-Hypodactylia Syndrome.
45: Hypohidrotic Ectodermal Dysplasia.
46: Hypomelanosis of Ito.
47: Hypophosphatasia.
48: Hypopituitarism.
49: I(1p), I(1q) Syndrome.
50: Idic(Yq) Syndrome.
51: Incontinentia Pigmenti.
52: Infantile Myofibromatosis.
53: Ivemark Syndrome.
54: Jarcho–Levin Syndrome.
55: Joubert Syndrome.
56: Kabuki Syndrome.
57: Kasabach–Merritt Syndrome.
58: KID Syndrome.
59: Klinefelter Syndrome.
60: Klippel–Feil Syndrome.
61: Klippel–Trenaunay Syndrome.
62: Kniest Dysplasia.
63: Larsen Syndrome.
64: Leopard Syndrome.
65: Lesch–Nyhan Syndrome.
66: Lethal Multiple Pterygium Syndrome.
67: Loeys–Dietz Syndrome.
68: Lowe Syndrome.
69: Marfan Syndrome.
70: McCune-Albright Syndrome.
71: Meckel–Gruber Syndrome.
72: Megalencephalic Leukoencephalopathy with Subcortical Cysts.
73: Menkes Disease.
74: Metachromatic Leukodystrophy.
75: Miller–Dieker Syndrome.
76: Mitochondrial Leber Hereditary Optic Neuropathy.
77: Möbius Syndrome.
78: Mowat–Wilson Syndrome.
79: Mucopolysaccharidosis I (MPS I).
80: Mucopolysaccharidosis II.
81: Mucopolysaccharidosis III.
82: Mucopolysaccharidosis IV.
83: Mucopolysaccharidosis VI.
84: Mucolipidosis II.
85: Mucolipidosis III.
86: Multiple Endocrine Neoplasia Syndromes.
87: Multiple Epiphyseal Dysplasia.
88: Multiple Pterygium Syndrome.
89: Myotonic Dystrophy Type I.
1: Nail-Patella Syndrome.
2: Neonatal Herpes Simplex Infection.
3: Nephrogenic Diabetes Insipidus.
4: Netherton Syndrome.
5: Neu–Laxova Syndrome.
6: Neural Tube Defects.
7: Neurofibromatosis 1.
8: Neurofibromatosis 2.
9: Noonan Syndrome.
10: Oblique Facial Cleft Syndrome.
11: Oligohydramnios Sequence.
12: Omphalocele.
13: Oral–Facial–Digital Syndrome.
14: Osteogenesis Imperfecta.
15: Osteopetrosis.
16: Osteopoikilosis.
17: Otopalatodigital Spectrum Disorders.
18: Pachyonychia Congenita.
19: Pallister–Killian Syndrome.
20: Phenylketonuria.
21: Pierre Robin Sequence.
22: Polycystic Kidney Disease, Autosomal Dominant Type.
23: Polycystic Kidney Disease: Autosomal Recessive Type.
24: Popliteal Pterygium Syndrome.
25: Prader–Willi Syndrome.
26: Progeria.
27: Prune Belly Syndrome.
28: Pseudoachondroplasia.
29: R(18) Syndrome.
30: Retinoid Embryopathy.
31: Rett Syndrome.
32: Rickets.
33: Rigid Spine Syndrome.
34: Roberts Syndrome.
35: Robinow Syndrome.
36: Rubinstein-Taybi Syndrome.
37: Saethre-Chotzen Syndrome.
38: Sagittal Craniosynostosis Associated with Chromosome Abnormalities with a Brief Review on Craniosynostosis.
39: Schizencephaly.
40: Schmid Metaphyseal Chondrodysplasia.
41: Seckel Syndrome.
42: Severe Combined Immune Deficiency.
43: Short Rib–Polydactyly Syndromes.
44: Sickle Cell Disease.
45: Silver–Russell Syndrome.
46: Sirenomelia.
47: Smith-Lemli-Opitz Syndrome.
48: Smith-Magenis Syndrome.
49: Sotos Syndrome.
50: Spinal Muscular Atrophy.
51: Spondyloepiphyseal Dysplasia.
52: Stickler Syndrome.
53: Sturge-Webber Syndrome.
54: Tay-Sachs Disease.
55: Tetrasomy 9p Syndrome.
56: Thalassemia.
57: Thanatophoric Dysplasia.
58: Thrombocytopenia-Absent Radius Syndrome.
59: Treacher-Collins Syndrome.
60: Trimethylaminuria.
61: Triploidy.
62: Trismus-Pseudocamptodactyly Syndrome.
63: Trisomy 8 Mosaicism Syndrome.
64: Trisomy 13 Syndrome.
65: Trisomy 18 Syndrome.
66: Tuberous Sclerosis.
67: Turner Syndrome.
68: Twin–Twin Transfusion Syndrome.
69: Ulnar-Mammary Syndrome.
70: Urofacial Syndrome.
71: VATER (VACTERL) Association.
72: Von Hippel–Lindau Disease.
73: Waardenburg Syndrome.
74: Weill–Marchesani Syndrome.
75: Williams Syndrome.
76: Wolf-Hirschhorn Syndrome.
77: X-Linked Agammaglobulinemia.
78: X-Linked Ichthyosis.
79: XX Male.
80: XXX Syndrome.
81: XXXXX Syndrome.
82: XXXXY Syndrome.
83: XY Female.
84: XYY Syndrome.