
Atlas of X-Linked Intellectual Disability Syndromes
Description
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Content
- Cover
- TABLE OF CONTENTS
- FOREWORD
- PREFACE
- AARSKOG SYNDROME
- ABIDI SYNDROME
- ADRENOLEUKODYSTROPHY
- AGENESIS OF THE CORPUS CALLOSUM, X-LINKED
- AHMAD SYNDROME
- AICARDI SYNDROME
- ALLAN-HERNDON-DUDLEY SYNDROME
- ALPHA-THALASSEMIA INTELLECTUAL DISABILITY (SEE ALSO ATRX-ASSOCIATED XLID)
- AP1S2-ASSOCIATED XLID
- APAK ATAXIA-SPASTIC DIPLEGIA SYNDROME
- ARMFIELD SYNDROME
- ARTS SYNDROME
- ARX-ASSOCIATED XLID
- ATAXIA-DEAFNESS-DEMENTIA, X-LINKED
- ATKIN-FLAITZ SYNDROME
- ATRX-ASSOCIATED XLID
- BERGIA CARDIOMYOPATHY
- BERTINI SYNDROME
- BÖRJESON-FORSSMAN-LEHMANN SYNDROME
- BRANCHIAL ARCH SYNDROME, X-LINKED
- CANTU SYNDROME
- CARPENTER-WAZIRI SYNDROME (SEE ALSO ATRX-ASSOCIATED XLID)
- CEREBRO-CEREBELLO-COLOBOMA SYNDROME
- CEREBRO-OCULO-GENITAL SYNDROME
- CEREBRO-PALATO-CARDIAC SYNDROME (SEE ALSO RENPENNING SYNDROME)
- CHARCOT-MARIE-TOOTH NEUROPATHY, COWCHOCK VARIANT
- CHARCOT-MARIE-TOOTH NEUROPATHY, IONASESCU VARIANT
- CHASSAING-LACOMBE CHONDRODYSPLASIA
- CHRISTIAN SYNDROME
- CHRISTIANSON SYNDROME
- CHUDLEY-LOWRY SYNDROME (SEE ALSO ATRX-ASSOCIATED XLID)
- CK SYNDROME
- CLARK-BARAITSER SYNDROME
- COFFIN-LOWRY SYNDROME
- CORNELIA DE LANGE SYNDROME, X-LINKED
- CRANIOFACIOSKELETAL SYNDROME
- CREATINE TRANSPORTER DEFICIENCY
- DUCHENNE MUSCULAR DYSTROPHY
- DYSKERATOSIS CONGENITA
- EPILEPSY-INTELLECTUAL DISABILITY IN FEMALES (EIDF)
- FITZSIMMONS SYNDROME
- FLNA-ASSOCIATED XLID
- FRAGILE X SYNDROME
- GIUFFRÈ-TSUKAHARA SYNDROME
- GLYCEROL KINASE DEFICIENCY
- GOLABI-ITO-HALL SYNDROME: (SEE ALSO RENPENNING SYNDROME)
- GOLDBLATT SPASTIC PARAPLEGIA SYNDROME
- GOLTZ SYNDROME
- GRAHAM ANOPHTHALMIA SYNDROME
- GUSTAVSON SYNDROME
- HALL OROFACIAL SYNDROME
- HEREDITARY BULLOUS DYSTROPHY, X-LINKED
- HOLMES-GANG SYNDROME (SEE ALSO ATRX-ASSOCIATED XLID)
- HOMFRAY SEIZURES-CONTRACTURES
- HYDE-FORSTER SYNDROME
- HYDRANENCEPHALY WITH ABNORMAL GENITALIA (SEE ALSO ARX-ASSOCIATED XLID)
- HYDROCEPHALY-CEREBELLAR AGENESIS SYNDROME
- HYDROCEPHALY-MASA SPECTRUM
- HYPOPARATHYROIDISM, X-LINKED
- INCONTINENTIA PIGMENTI
- JUBERG-MARSIDI-BROOKS SYNDROME
- KANG SYNDROME
- LENZ MICROPHTHALMIA SYNDROME
- LESCH-NYHAN SYNDROME
- LISSENCEPHALY AND ABNORMAL GENITALIA, X-LINKED (SEE ALSO ARX-ASSOCIATED XLID)
- LISSENCEPHALY, X-LINKED
- LOWE SYNDROME
- LUJAN SYNDROME
- MARTIN-PROBST SYNDROME
- MEHMO SYNDROME
- MENKES SYNDROME
- MIDAS SYNDROME
- MILES-CARPENTER SYNDROME
- MOHR-TRANEBJAERG SYNDROME
- MONOAMINE OXIDASE-A DEFICIENCY
- MUCOPOLYSACCHARIDOSIS IIA
- MYOTUBULAR MYOPATHY
- N-ALPHA-ACETYLTRANSFERASE DEFICIENCY
- NANCE-HORAN SYNDROME
- NORRIE DISEASE
- OPITZ FG SYNDROME
- OPTIC ATROPHY, X-LINKED
- ORAL-FACIAL-DIGITAL SYNDROME I
- ORNITHINE TRANSCARBAMOYLASE DEFICIENCY
- OTOPALATODIGITAL SYNDROME I (SEE ALSO FLNA-ASSOCIATED XLID)
- OTOPALATODIGITAL SYNDROME II (SEE ALSO FLNA-ASSOCIATED XLID)
- PAINE SYNDROME
- PALLISTER W SYNDROME
- PARTINGTON SYNDROME (SEE ALSO ARX-ASSOCIATED XLID)
- PELIZAEUS-MERZBACHER SYNDROME
- PERIVENTRICULAR NODULAR HETEROTOPIA (SEE ALSO FLNA-ASSOCIATED XLID)
- PETTIGREW SYNDROME
- PHOSPHOGLYCERATE KINASE DEFICIENCY
- PLOTT SYNDROME
- PORTEOUS SYNDROME (SEE ALSO RENPENNING SYNDROME)
- PPM-X
- PRIETO SYNDROME
- PROUD SYNDROME (SEE ALSO ARX-ASSOCIATED XLID)
- PYRUVATE DEHYDROGENASE DEFICIENCY
- RENPENNING SYNDROME
- RET T SYNDROME
- RETT-LIKE SEIZURES-HYPOTONIA
- ROIFMAN SYNDROME
- SAY-MEYER SYNDROME
- SCHIMKE SYNDROME
- SHASHI SYNDROME
- SHRIMPTON SYNDROME
- SIMPSON-GOLABI-BEHMEL SYNDROME
- SMITH-FINEMAN-MYERS SYNDROME
- SNYDER-ROBINSON SYNDROME
- STOCCO DOS SANTOS SYNDROME
- STOLL SYNDROME
- SUTHERLAND-HAAN SYNDROME (SEE ALSO RENPENNING SYNDROME)
- TARP SYNDROME
- TELECANTHUS-HYPOSPADIAS SYNDROME
- TURNER XLID (SEE ALSO AP1S2-ASSOCIATED XLID)
- URBAN SYNDROME
- VACTERL-HYDROCEPHALUS SYNDROME
- VASQUEZ SYNDROME
- WAISMAN-LAXOVA SYNDROME
- WARKANY SYNDROME
- WIEACKER-WOLFF SYNDROME
- WILSON-TURNER SYNDROME
- WITTWER SYNDROME
- XLID-ARCH FINGERPRINTS-HYPOTONIA SYNDROME (SEE ALSO ATRX-ASSOCIATED XLID)
- XLID-ATAXIA-APRAXIA
- XLID-ATAXIA-DEMENTIA
- XLID-BLINDNESS-SEIZURES-SPASTICITY
- XLID-CHOREOATHETOSIS
- XLID-CHOROIDEREMIA-ECTODERMAL DYSPLASIA
- XLID-CLEFT LIP/CLEFT PALATE
- XLID-EPILEPSY (XIDE)
- XLID-HYDROCEPHALY-BASAL GANGLIA CALCIFICATIONS (SEE ALSO AP1S2-ASSOCIATED XLID)
- XLID-HYPOGAMMAGLOBULINEMIA
- XLID-HYPOGONADISM-TREMOR
- XLID-HYPOSPADIAS
- XLID-HYPOTONIA-RECURRENT INFECTIONS
- XLID-ICHTHYOSIS-HYPOGONADISM
- XLID-INFANTILE SPASMS (SEE ALSO ARX-ASSOCIATED XLID)
- XLID-ISOLATED GROWTH HORMONE DEFICIENCY
- XLID-MACROCEPHALY
- XLID-MACROCEPHALY-MACROORCHIDISM
- XLID-MICROCEPHALY-TESTICULAR FAILURE
- XLID-NAIL DYSTROPHY-SEIZURES
- XLID-NYSTAGMUS-SEIZURES
- XLID-PANHYPOPITUITARISM
- XLID-PRECOCIOUS PUBERT Y
- XLID-PSORIASIS
- XLID-RETINITIS PIGMENTOSA
- XLID-ROLANDIC SEIZURES
- XLID-SPASTIC PARAPLEGIA, TYPE 7
- XLID-SPASTIC PARAPLEGIA-ATHETOSIS
- XLID-SPONDYLOEPIMETAPHYSEAL DYSPLASIA
- XLID-THYROID APLASIA-CUTIS VERTICIS GYRATA
- XLID WITH THYROXINE-BINDING GLOBULIN DEFICIENCY
- YOUNG-HUGHES SYNDROME
- APPENDICES
- I. GENES INVOLVED IN X-LINKED INTELLECTUAL DISABILITY (BY ORDER OF DISCOVERY)
- II. XLID SYNDROMES WITH MICROCEPHALY
- III. XLID SYNDROMES WITH MACROCEPHALY
- IV. XLID SYNDROMES WITH OCULAR ANOMALIES AND/OR VISUAL IMPAIRMENT
- V. XLID SYNDROME WITH HEARING LOSS
- VI. XLID SYNDROMES WITH FACIAL CLEFTING
- VII. XLID SYNDROMES WITH CARDIAC MALFORMATIONS OR OTHER CARDIOVASCULAR ABNORMALITIES
- VIII. XLID SYNDROMES WITH UROGENITAL ANOMALIES
- IX. XLID SYNDROMES WITH NEURONAL MIGRATION DISTURBANCE
- X. XLID SYNDROMES WITH SPASTIC PARAPLEGIA
- XI. XLID SYNDROMES WITH SEIZURES
- XII. XLID SYNDROMES WITH HYPOTONIA
- XIII. XLID SYNDROMES PREDOMINANTLY AFFECTING FEMALES
- XIV. DUPLICATION OF XLID GENES AND REGIONS OF THE X-CHROMOSOME GENOME
- XV. X-INACTIVATION
- XVI. SYNDROMAL XLID GENES
- XVII. SYNDROMAL XLID (LINKAGE LIMITS)
- XVIII. NONSYNDROMAL XLID FAMILIES
- XIX. NONSYNDROMAL XLID FAMILIES
- INDEX
- A
- B
- C
- D
- E
- F
- G
- H
- I
- J
- K
- L
- M
- N
- O
- P
- R
- S
- T
- U
- V
- W
- X
- Y
- Z
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