Discriminative features in three autosomal recessive cutis laxa syndromes: Cutis laxa IIA, cutis laxa IIB, and geroderma osteoplastica

Discriminative features in three autosomal recessive cutis laxa syndromes: Cutis laxa IIA, cutis laxa IIB, and geroderma osteoplastica

10.3390/ijms18030635

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Bibliographic Details
Main Authors:	Kariminejad, A, Afroozan, F, Bozorgmehr, B, Ghanadan, A, Akbaroghli, S, Khorshid, H.R.K, Mojahedi, F, Setoodeh, A, Loh, A, Tan, Y.X, Escande-Beillard, N, Malfait, F, Reversade, B, Gardeitchik, T, Morava, E
Other Authors:	PAEDIATRICS
Format:	Review
Published:	MDPI 2020
Subjects:	autosomal recessive cutis laxa 2a autosomal recessive cutis laxa 2b cataract cognition congenital hip dislocation cutis laxa geroderma osteodysplastica human lipodystrophy long philtrum microcephaly muscle hypotonia osteopenia palpebral fissure phenotype Review short stature wrinkle adult Bone Diseases case report child differential diagnosis dwarfism female infant male preschool child Skin Diseases, Genetic syndrome Adult Child Child, Preschool Cutis Laxa Diagnosis, Differential Dwarfism Female Humans Infant Male Phenotype Syndrome
Online Access:	https://scholarbank.nus.edu.sg/handle/10635/183539
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Institution:	National University of Singapore

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