Micromelic dwarfism - Humerus, femur and tibia type

L. I. Al-Gazali; M. Bakir; Z. Hamid; D. Nath; D. Haas

doi:10.1097/00019605-200101000-00005

Micromelic dwarfism - Humerus, femur and tibia type

L. I. Al-Gazali, M. Bakir, Z. Hamid, D. Nath, D. Haas

Research output: Contribution to journal › Article › peer-review

2 Citations (Scopus)

Abstract

We report a baby with severe micromelic dwarfism characterized by severe shortening of the humeri, femora and tibiae with hypoplastic radii, ulnae and fibulae which are of normal shape. We suggest that this case is similar to the case reported by Baxova et al [(1993), Paediatr Radiol 23:446-449] confirming the identity of this new bone dysplasia.

Original language	English
Pages (from-to)	25-28
Number of pages	4
Journal	Clinical Dysmorphology
Volume	10
Issue number	1
DOIs	https://doi.org/10.1097/00019605-200101000-00005
Publication status	Published - 2001

Keywords

Bone dysplasia
Micromelic dwarfism

ASJC Scopus subject areas

Pediatrics, Perinatology, and Child Health
Anatomy
Pathology and Forensic Medicine
Genetics(clinical)

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10.1097/00019605-200101000-00005

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abstract = "We report a baby with severe micromelic dwarfism characterized by severe shortening of the humeri, femora and tibiae with hypoplastic radii, ulnae and fibulae which are of normal shape. We suggest that this case is similar to the case reported by Baxova et al [(1993), Paediatr Radiol 23:446-449] confirming the identity of this new bone dysplasia.",

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AU - Al-Gazali, L. I.

AU - Bakir, M.

AU - Hamid, Z.

AU - Nath, D.

AU - Haas, D.

PY - 2001

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N2 - We report a baby with severe micromelic dwarfism characterized by severe shortening of the humeri, femora and tibiae with hypoplastic radii, ulnae and fibulae which are of normal shape. We suggest that this case is similar to the case reported by Baxova et al [(1993), Paediatr Radiol 23:446-449] confirming the identity of this new bone dysplasia.

AB - We report a baby with severe micromelic dwarfism characterized by severe shortening of the humeri, femora and tibiae with hypoplastic radii, ulnae and fibulae which are of normal shape. We suggest that this case is similar to the case reported by Baxova et al [(1993), Paediatr Radiol 23:446-449] confirming the identity of this new bone dysplasia.

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KW - Micromelic dwarfism

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Micromelic dwarfism - Humerus, femur and tibia type

Abstract

Keywords

ASJC Scopus subject areas

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