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CONDRODISPLASIA PUNCTATA RIZOMLICA PDF

Rhizomelic chondrodysplasia punctata is a rare developmental brain disorder characterized by systemic shortening of the proximal bones (i.e. rhizomelia). A number sign (#) is used with this entry because of evidence that rhizomelic chondrodysplasia punctata type 1 (RCDP1) is caused by homozygous or. Rhizomelic chondrodysplasia punctata (RCDP) is a peroxisomal disorder characterized by disproportionately short stature primarily affecting the proximal parts.

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Rhizomelic chondrodysplasia punctate RCDP is a rare autosomal recessive peroxisomal disease. The main features of the disease are shortening of the proximal long bones, punctate calcifications located in the epiphyses of long bones and in soft tissues around joints and vertebral column, vertebral clefting, dysmorphic face, and severe growth retardation, whereas cervical spinal stenosis may also rarely be present.

Imaging of the brain and spinal cord in patients with this disorder may aid prognosis and guide management decisions. We report the newborn diagnosed as CDP with cervical stenosis.

Our aim is to discuss current knowledge on etiopathogenesis as well as radiological and clinical symptoms of diseases associated with CDP. Rhizomelic chondrodysplasia punctata RCDP is a rare disorder of peroxisomal metabolism, with an estimated incidence 1: There are 3 genetic subtypes. RCP type 2 arises secondary to mutations in the acyl-CoA: The main features of the disease are shortening of the proximal long bones, punctate calcifications in the metaphysis and epiphysis of long bones and the thoracic and lumbar vertebrae, dysmorphic face, and severe growth retardation.

Cervical stenosis is very rarely reported in rhizomelic CDP cases puncatta 13 ]. Because of underlying vertebral abnormalities, spinal stenosis, often seen together with brachytelephalangic chondrodysplasia punctata, can cause progressive neurological findings.

Rhizomelic chondrodysplasia punctata – Wikipedia

Here, we report a case of RCDP with cervical spinal stenosis in newborn. The term infant was admitted to the neonatology department because of its atypical facial appearance and extremity anomalies at the 2nd hour of her life.

The female infant was born at 38 weeks of gestation from the fourth pregnancy of a healthy year-old mother and a year-old related father. The mother was under routine prenatal follow-up during pregnancy. She did not have any chronic disease and there was no history of exposure to any known embryopathic agents and, in particular, no warfarin therapy or alcohol use had been given.

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Prenatal ultrasonographic assessments reported proximal limb shortening. The mother had two miscarriages, as well as a baby with skeletal abnormalities who was aborted at 22 gestational weeks and a healthy male child.

There was shortness of the upper extremities and flexion contractures in all extremities. In the skeletal survey performed, there were proximal shortness, thick and short diaphyses, and large and irregular metaphyses in the long bones and normal fingers. The radiological findings of the patient were compatible with CDP with punctate calcifications in the epiphyses and coronal clefts in the vertebral bodies Figure 1. Complete blood count, biochemical parameters, and abdominal ultrasonography were all normal.

Cavum vergae and minimal dilatation in the right ventricle were observed on cranial ultrasonography.

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On the cranial MR investigation, both lateral ventricles and the third ventricle were found to be larger than normal and there was atrophy in the left temporal lobe. Bilateral nuclear cataract was seen on the ophthalmological examination.

Her karyotype test was normal rizomlifa, XX. Blood amino acid and urinary organic acid levels were unremarkable, and anti-DNA and ANA tests condordisplasia her mother revealed negative results.

Further biochemical studies showed high phytanic acid 9. RCDP1 was diagnosed based on clinical, biochemical, and radiological criteria. Parents were informed about this disease, and genetic counseling was given. She was operated at condrodiisplasia age of 1 month for bilateral cataract.

She has been in follow-up for spinal stenosis and probable nutritional problems. Echocardiography was planned to monitor the size of heart defect after 6 months.

Chondrodysplasia punctata CDP is a rarely occurring skeletal dysplasia characterized by stippled, punctuate calcifications around joints and within cartilages [ 1 ].

CDP is associated with a number of disorders, including inborn errors of metabolism, involving peroxisomal and cholesterol pathways, embryopathy, and chromosomal abnormalities [ 2 — 7 ]. Several classification systems of the different types of CDP have been suggested earlier.

More recently, the biochemical and molecular basis of a number of CDP syndromes has recently been elucidated and a new aetiological classification has emerged [ 2 ]. Rhizomelic chondrodysplasia punctata is a disorder caused by abnormal peroxisomal function which can be mediated both through disorders of biosynthesis, for example, peroxisomal assembly RDCP1and by single enzyme defects, affecting plasmalogen synthesis RCDP2, RCDP3.

Growth and development are severely restricted. Life expectancy is considerably reduced [ 128 ]. The following situations should be considered in the differential diagnosis of CDP: There was no history of maternal drug or alcohol use and no symptoms or positive laboratory test that indicated autoimmunological disease in the mother.

Because our case had high phytanic acid level and autosomal recessive inheritance, she was diagnosed as RCDP1.

Spinal stenosis is a frequent sign of bone dysplasia, while it is rarely reported in rhizomelic CDP cases [ 11 — 13 ]. Cervical spinal stenosis, which in some cases leads to cord compression and myelopathy, has been described in chondrodysplasia punctate of rhizomelic, brachytelephalangic, and Conradi-Hunermann types [ 13 ]. Because patients with RCDP often demonstrate upper and lower extremity spasticity in the absence of spinal cord involvement, diagnosis of cervical spinal stenosis secondary to RCDP may be difficult.

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In addition, it is sometimes hard to establish the clinical finding of spasticity because multiple joints have limited range of motion [ 14 ]. Also, a recent study found an association between overall disease severity and the presence of abnormalities on brain magnetic resonance imaging [ 15 ].

Because neuroimaging can provide prognostic information, it is important to look for cervical stenosis in these patients. These patients may be screened with conventional radiographs of the cervical spine and cases with radiographs suggestive of spinal stenosis and physical examinations compatible with myelopathy may be further evaluated with MRI when clinically indicated [ 14 ]. In our case, cervical stenosis was detected on the spinal MRI investigations performed for this purpose.

But our patient who had cervical stenosis still has no neurological findings. Spasticity, psychomotor retardation, growth retardation, seizures, thermoregulatory instability, feeding difficulty, recurrent otitis media, and pneumonia have been reported in CDP cases [ 11 ].

So, our patient was described as mildly affected. Prenatal diagnosis of RCDP is possible from the first trimester onwards by demonstration of peroxisomal dysfunction in cultured chorionic villous or amniotic fluid cells [ 3 ]. Genetic counseling was given to parents of our case. In conclusion, cervical spinal stenosis is a rare anomaly in rhizomelic chondrodysplasia punctata cases, which may cause neurological findings.

The authors declare that there is no conflict of interests regarding the publication of this paper. Case Reports in Medicine. Indexed in Web of Science. Subscribe to Table of Contents Alerts. Table of Contents Alerts. Abstract Rhizomelic chondrodysplasia punctate RCDP is a rare autosomal recessive peroxisomal disease.

Introduction Rhizomelic chondrodysplasia punctata RCDP is a rare disorder of peroxisomal metabolism, with an estimated incidence 1: Case The term infant was admitted to the neonatology department because of its atypical facial appearance and extremity anomalies at the 2nd hour of her life.

Proximal shortness, thick and short diaphyses, large and irregular metaphyses, and punctate calcifications in the epiphyses in the long bones and coronal clefts not included in the vertebral bodies. View at Google Scholar A.