What is Michael syndrome?

Michels syndrome is a syndrome characterised by intellectual disability, craniosynostosis, blepharophimosis, ptosis, epicanthus inversus, highly arched eyebrows, and hypertelorism.

What causes Meckel syndrome?

Meckel syndrome can be caused by changes (mutations) in thirteen genes: B9D1, B9D2, CC2D2A, CEP290, MKS1, RPGRIP1L, TCTN2, TCTN3, TMEM67, TMEM107, TMEM216, TMEM231 and TMEM237. Mutations in these 13 genes account for 75 percent of all cases; the remaining 25 percent have unknown genetic causes.

What is Meckel's syndrome?

Meckel syndrome is a very severe disorder that is characterized by multiple cysts on the kidneys, protrusion of a portion of the brain through an opening in the skull (occipital encephalocele), and extra fingers or toes (polydactyly).

How common is Meckel-Gruber syndrome?

Meckel syndrome affects 1 in 13,250 to 1 in 140,000 people worldwide. It is more common in certain populations; for example, the condition affects about 1 in 9,000 people of Finnish ancestry and about 1 in 3,000 people of Belgian ancestry.

How is Meckel-Gruber syndrome diagnosed?

Infants with Meckel-Gruber syndrome can be diagnosed based on their appearance at birth, or by ultrasound before birth. Most cases diagnosed through ultrasound are diagnosed in the second trimester. However, a skilled technician may be able to identify the condition during the first trimester.

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What is Miller dieker syndrome?

Miller-Dieker syndrome is a condition characterized by a pattern of abnormal brain development known as lissencephaly. Normally the exterior of the brain (cerebral cortex ) is multi-layered with folds and grooves. People with lissencephaly have an abnormally smooth brain with fewer folds and grooves.

Where is Meckel's diverticulum located?

Meckel's diverticulum is a small pouch in the wall of the intestine, near the junction of the small and large intestines. The pouch is a remnant of tissue from the prenatal development of the digestive system.

What causes Meckel-Gruber?

Meckel–Gruber syndrome (MKS) is a lethal autosomal recessive congenital anomaly syndrome caused by mutations in genes encoding proteins that are structural or functional components of the primary cilium.

What is the life expectancy of a child with Joubert syndrome?

Mean age of death in this cohort was 7.2 years, and the most prevalent causes of death were respiratory failure (35%), particularly in individuals younger than 6 years, and kidney failure (37.5%), which was more common in older individuals.

What is associated with Meckel-Gruber?

Cystic dysplasia of the kidneys is the most constant and characteristic feature of Meckel-Gruber syndrome. Associated abnormalities include oral clefting, genital anomalies; CNS malformations, including Dandy-Walker, Arnold-Chiari malformation, and liver fibrosis.

What are symptoms of Jacobsen syndrome?

These include small and low-set ears, widely set eyes (hypertelorism ) with droopy eyelids (ptosis ), skin folds covering the inner corner of the eyes (epicanthal folds ), a broad nasal bridge , downturned corners of the mouth , a thin upper lip , and a small lower jaw .

How long does a Meckel scan take?

Here are some things you might expect to happen during your child's Meckel's scan. The entire scan should take about 30 to 60 minutes. Typically, doctors don't use sedation during the procedure, so your child should be awake.

Is Aicardi syndrome hereditary?

Inheritance. Nearly all known cases of Aicardi syndrome are sporadic, which means that they are not passed down through generations and occur in people with no history of the disorder in their family. The disorder is believed to result from new gene mutations.

Is Joubert syndrome a disability?

Social Security Disability Benefits

While Joubert Syndrome does not have it's own listing, it does qualify under two other listings: 111.06 Motor Dysfunction (due to any neurological disorder) or 111.07B Cerebral Palsy.

Is Joubert syndrome curable?

There is no cure for Joubert syndrome.

Is Joubert syndrome hereditary?

Joubert syndrome typically has an autosomal recessive pattern of inheritance, which means both copies of a gene in each cell have mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they usually do not show signs and symptoms of the condition.

Is Meckel's diverticulum serious?

These ulcers can bleed or perforate (rupture), causing intestinal waste products to leak into the abdomen. This can result in a serious abdominal infection called peritonitis. Meckel's diverticulum can also cause intestinal obstruction.

Is Meckel's diverticulum life threatening?

Erratic symptoms can make the condition difficult for your doctor to diagnose. In rare cases, excessive bleeding from Meckel's diverticulum may occur and become life-threatening. If this happens, emergency surgery may be needed to remove the diverticulum.

What is the most common complication of Meckel's diverticulum?

The major complications are hemorrhage, obstruction, intussusception, diverticulitis and perforation. Bleeding is the most common complication occurring in children, and it typically presents as hematochezia. The hemorrhage is a result of heterotopic gastric mucosa leading to ulceration.

What is Pallister Killian syndrome?

This condition is characterized by extremely weak muscle tone (hypotonia) in infancy and early childhood, intellectual disability, distinctive facial features, sparse hair, areas of unusual skin coloring (pigmentation), and other birth defects.

What is Schinzel giedion syndrome?

General Discussion. Schinzel Giedion syndrome (SGS) is a very rare genetic disorder with characteristic facial features, skeletal abnormalities, and obstruction of the tube that carries urine from the kidney to the bladder (ureter). This obstruction may lead to enlarged and damaged kidneys (hydronephrosis).

What is Langer giedion syndrome?

Langer-Giedion syndrome is a very uncommon autosomal dominant genetic disorder caused by the deletion of chromosomal material. It is characterized by multiple bony exostosis, short stature, mental retardation, and typical facial features.

Can Aicardi syndrome be cured?

There is no cure for Aicardi syndrome nor is there a standard course of treatment. Treatment generally involves medical management of seizures and programs to help parents and children cope with developmental delays.

Can people with Aicardi syndrome talk?

Nearly all children with the disorder have some type of intellectual disability or developmental delay. However, other symptoms can vary significantly depending on the person. Some children with Aicardi syndrome can speak in short sentences and walk by themselves.

Is Aicardi syndrome a neurological disorder?

Aicardi syndrome is a rare congenital disorder that causes malformations affecting the brain, eyes and other body parts. Children typically experience lifelong challenges with disabilities, seizures and other medical issues.