Dysmorphism, variable overgrowth, normal bone age, and severe developmental delay: A "Sotos-like" syndrome? [9]

Journal of Medical Genetics

Volumn 39, Issue 2, 2002, Pages 148-152

  Amiel, J ^a   Faivre, L ^a   Wilson, L ^a   Le Merrer, M ^a   Munnich, A ^a   Winter, R ^a   Lyonnet, S ^a   Cormier Daire, V ^a   Stumm, M ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

VIGABATRIN;

AMNIOCENTESIS; BONE AGE; CHILD; CHILD GROWTH; CLINICAL ARTICLE; CLINICAL FEATURE; CORPUS CALLOSUM AGENESIS; ELECTROENCEPHALOGRAM; FACE DYSMORPHIA; FACIES; FEMALE; HUMAN; HYPSARRHYTHMIA; KARYOTYPING; LETTER; MACROCEPHALY; MALE; MONOZYGOTIC TWINS; NUCLEAR MAGNETIC RESONANCE IMAGING; PATENT DUCTUS ARTERIOSUS; POSTNATAL GROWTH; PRIORITY JOURNAL; PSYCHOMOTOR DEVELOPMENT; SEIZURE; SOTOS SYNDROME; UNIPARENTAL DISOMY; VESICOURETERAL REFLUX;

ACROMEGALY; AGE FACTORS; BONE DEVELOPMENT; BRAIN DISEASES; CHILD; CHILD, PRESCHOOL; DEVELOPMENTAL DISABILITIES; DIAGNOSIS, DIFFERENTIAL; FEMALE; GIGANTISM; GROWTH DISORDERS; HUMANS; MALE; SYNDROME;

EID: 0036173053     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (12)

1. Cerebral gigantism in childhood
2. Sotos syndrome
3. Sotos syndrome: A study of the diagnostic criteria and natural history
4. Identical twins discordant for Sotos syndrome
5. Apparent Sotos syndrome (cerebral gigantism) in a child with trisomy 20p11.2-p12.1 mosaicism
6. No evidence for uniparental disomy as a common cause of Sotos syndrome
7. The neuroimaging findings in Sotos syndrome
8. Macrocephaly-cutis marmorata telangiectatica congenita: Report of five patients and a review of the literature
9. Sotos syndrome associated with West syndrome and a visual disorder
10. Sotos syndrome and cutis laxa
11. Overgrowth, congenital hypotonia, nystagmus, strabismus, and mental retardation: Variant of dominantly inherited Sotos sequence?