Achondroplasia is an autosomal dominant disease which is characterized by limb shortening and narrow trunk, and macrocephaly. Women with achondroplasia suffer from infertility, menorrhagia, dysmenorrhoea, leiomyomata and early menopause. Our case was a 26-year-old woman with achondroplasia who had scoliosis and osteoporosis. She referred to our clinic at 9 weeks of gestation and had all screenings completely. She had a single female fetus with no abnormalities. She had an emergent due to rupture of membranes at 37 weeks and 3 days under general anesthesia. The neonate had no complications. The first minute Apgar score was 9 and 5th-minute Apgar score were 10. Umbilical artery Ph was 7.26 and birth weight was 3140. A woman with achondroplasi...
Otocephaly is a rare lethal syndrome of microstomia, aglossia, agnathia, and synotia. This male infa...
Achondroplasia is caused by the failure of bone growth at the cartilaginous end plate and is the mos...
Achondroplasia is a rare genetic disorder resulting in short-limb skeletal dysplasia. We present the...
Pregnancy in women with achondroplasia presents major challenges for anaesthetists and obstetricians...
ABSTRACT Achondroplasia, a skeletal dysplasia has an incidence of 1 in 15000 to 1 in 30000 live birt...
Achondroplasia is the result of a mutation in the gene encoding the type 3 receptor for a fibroblast...
Achondrogenesis, is a form of skeletal displazia with the characteristic features of severe shorteni...
OBJECTIVES: To characterize the natural history of 39 achondroplastic patients diagnosed by clinical...
A 45-year-old woman with short stature and primary amenorrhoea was admitted during a health-screenin...
Otocephaly is characterized by agenesis or severe hypogenesis of the mandible or agnathia, synotia (...
Arthrogryposis Multiplex Congenita (AMC) is a symptom complex of congenital joint contractures assoc...
Achondrogenesis is a lethal congenital chondrodystrophy characterized by extreme micromelia, small ...
Achondroplasia is a rare genetic disorder resulting in short-limb skeletal dysplasia. We present the...
Achondroplasia is a rare genetic disorder resulting in short-limb skeletal dysplasia. We present the...
Copyright © 2015 Esther Perez-Carbajo et al. This is an open access article distributed under the Cr...
Otocephaly is a rare lethal syndrome of microstomia, aglossia, agnathia, and synotia. This male infa...
Achondroplasia is caused by the failure of bone growth at the cartilaginous end plate and is the mos...
Achondroplasia is a rare genetic disorder resulting in short-limb skeletal dysplasia. We present the...
Pregnancy in women with achondroplasia presents major challenges for anaesthetists and obstetricians...
ABSTRACT Achondroplasia, a skeletal dysplasia has an incidence of 1 in 15000 to 1 in 30000 live birt...
Achondroplasia is the result of a mutation in the gene encoding the type 3 receptor for a fibroblast...
Achondrogenesis, is a form of skeletal displazia with the characteristic features of severe shorteni...
OBJECTIVES: To characterize the natural history of 39 achondroplastic patients diagnosed by clinical...
A 45-year-old woman with short stature and primary amenorrhoea was admitted during a health-screenin...
Otocephaly is characterized by agenesis or severe hypogenesis of the mandible or agnathia, synotia (...
Arthrogryposis Multiplex Congenita (AMC) is a symptom complex of congenital joint contractures assoc...
Achondrogenesis is a lethal congenital chondrodystrophy characterized by extreme micromelia, small ...
Achondroplasia is a rare genetic disorder resulting in short-limb skeletal dysplasia. We present the...
Achondroplasia is a rare genetic disorder resulting in short-limb skeletal dysplasia. We present the...
Copyright © 2015 Esther Perez-Carbajo et al. This is an open access article distributed under the Cr...
Otocephaly is a rare lethal syndrome of microstomia, aglossia, agnathia, and synotia. This male infa...
Achondroplasia is caused by the failure of bone growth at the cartilaginous end plate and is the mos...
Achondroplasia is a rare genetic disorder resulting in short-limb skeletal dysplasia. We present the...